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Adac Laboratories

Country not established

Devices
88
FDA recalls
6

What Adac Laboratories makes

Adac Laboratories manufactures medical imaging systems and software, including nuclear medicine imaging computers, digital processing systems, and cardiology modules. Their product portfolio also encompasses quantitative blood pool SPECT systems, imaging systems, and additional software solutions.

The company's devices are regulated as Class I and Class II medical devices and are listed in the FDA 510(k) registry. Adac Laboratories is based in the United States.

AI-generated from registry data, 26 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue88

Newest first, rows 51-88 of 88

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  • Vertex Epic Mcd Ref K952684

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Thyrus Ref K930283

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Pegasys Intouch Ref K974474

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Modified Adac Nuclear Medicine Gamma Camera Ref K900689

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Radiation Oncology System Ref K782005

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • 3D-Mspect Ref K980867

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Adac Model Dps-6100 Multi Modality Digital Procesing Systems Ref K827572

    Active Regimes: 510(k) Registry: 510(k) Class:—

  • P3IMRT Tm Ref K002237

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • PINNACLE3 Radiation Therapy Planning System Ref K041577 Open recall

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Adac S315 Ref K921296

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Cirrus Gamma Camera Ref K913471

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Autoquant Plus Ref K040326

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Syntegra Ref K041182

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • PINNACLE3 Radiation Therapy Planning System Ref K032724

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • C-Equal(Ceders-Emory Quantitive Analysis) Ref K932745

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Autospect Plus With Instill Motion Correction Ref K992317

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Dps-3300 Micro Nuclear Medicine Imaging Computer Ref K844783

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Adac Tomography Option Ref K791055

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Linear Accelerator Multiple Exl 3-4-6 Ref K840136

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Bi-Plane Digital Fluorography DFX7000 Ref K834286

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Genesys Ii Ref K922080

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Jetstream Workspace Ref K061029

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Adac Xl-Plan-Pc Ref K920041

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Viewpoint Ref K882205

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Adac Model Arc-St, Pc Style Data Processing System Ref K874473

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Apollo Gamma Camera System Ref K062298 Open recall

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Digital Radiography Sys-DPS7100 Ref K834287

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Dicom 3.0 Software Version 2.0 Ref K973239

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Dtv-4112 Fluoroscopic Television Camera Ref K871127

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Autospecs Ref K042903

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Option U1 For The Dps-Plus System Ref K915305

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Multi-View Processor (Mvp) Ref K931184

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Adac Models Xl-Plan 23 & Xl-Plan 73 Ref K851041

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Inspect/Prospect Ref K952564

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Digital Processing System Ref K840052

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Rtp-5000 Ref K813439

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Adac Dps-4070 Digital Radiography Sys Ref K843708

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Pinnacle 3 Ref K926008

    Active Regimes: 510(k) Registry: 510(k) Class:II

Rows 51-88 of 88

Showing 51-88 of 88

FDA recalls6

Recalls are matched to the firm by name. FDA recall data as of 22 Oct 2026.

FDA recall records list 6 recalls initiated by Adac Laboratories, initiated on 2004-03-03. By recorded status: 6 terminated. The reasons filed fall into these groups: software or firmware. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.

Generated automatically from FDA recall records, as a summary of the records listed below. It describes what the records state and is not an assessment of this manufacturer.

  • 2004

    • 3 Mar 2004 Z-0911-04 Unclassified (pre-2012) Terminated A software defect, relating to the motorized wedge functionality when using an Elekta linear accelerator, can result in incorrect dose delivery to the patient. Also, dose delivery in the wrong location may occur when using a Elekta Leksell headframe. Distribution: The recalled products were shipped to consignees located nationwide the United States and in Australia, Canada, China,…
      Full distribution text The recalled products were shipped to consignees located nationwide the United States and in Australia, Canada, China, and Korea.
      Submission number: K032724
    • 3 Mar 2004 Z-0912-04 Unclassified (pre-2012) Terminated A software defect, relating to the motorized wedge functionality when using an Elekta linear accelerator, can result in incorrect dose delivery to the patient. Also, dose delivery in the wrong location may occur when using a Elekta Leksell headframe. Distribution: The recalled products were shipped to consignees located nationwide the United States and in Australia, Canada, China,…
      Full distribution text The recalled products were shipped to consignees located nationwide the United States and in Australia, Canada, China, and Korea.
    • 3 Mar 2004 Z-0913-04 Unclassified (pre-2012) Terminated A software defect, relating to the motorized wedge functionality when using an Elekta linear accelerator, can result in incorrect dose delivery to the patient. Also, dose delivery in the wrong location may occur when using a Elekta Leksell headframe. Distribution: The recalled products were shipped to consignees located nationwide the United States and in Australia, Canada, China,…
      Full distribution text The recalled products were shipped to consignees located nationwide the United States and in Australia, Canada, China, and Korea.
    • 3 Mar 2004 Z-0914-04 Unclassified (pre-2012) Terminated A software defect, relating to the motorized wedge functionality when using an Elekta linear accelerator, can result in incorrect dose delivery to the patient. Also, dose delivery in the wrong location may occur when using a Elekta Leksell headframe. Distribution: The recalled products were shipped to consignees located nationwide the United States and in Australia, Canada, China,…
      Full distribution text The recalled products were shipped to consignees located nationwide the United States and in Australia, Canada, China, and Korea.
    • 3 Mar 2004 Z-0915-04 Unclassified (pre-2012) Terminated Dose delivery in the wrong location may occur when using a Elekta Leksell headframe. Distribution: The recalled products were shipped to consignees located nationwide the United States and in Australia, Canada, China,…
      Full distribution text The recalled products were shipped to consignees located nationwide the United States and in Australia, Canada, China, and Korea.
    • 3 Mar 2004 Z-0916-04 Unclassified (pre-2012) Terminated Dose delivery in the wrong location may occur when using a Elekta Leksell headframe. Distribution: The recalled products were shipped to consignees located nationwide the United States and in Australia, Canada, China,…
      Full distribution text The recalled products were shipped to consignees located nationwide the United States and in Australia, Canada, China, and Korea.