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Diagnostic Technology, Inc.

United StatesFDA applicant, unverified

Devices
28

Catalogue28

Newest first, rows 1-28 of 28

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  • Digital Radiography System Ref K827289

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

  • Picoscale Blood Cell Counter, Model Ps-5 Ref K860166

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

  • Sickle-Check Ref K820037

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

  • Laser-Cal Ref K811063

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

  • Lyme-Check(Tm) Test Kit Ref K896378

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

  • Resubmitted Ebv/Igm-Check Test Kit Ref K890639

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

  • Bhcg-Check Ref K834346

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

  • Picoscal Blood Cell Counter Ps-4 Ref K842140

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

  • Hsv-Check(Tm) Test Kit Ref K890819

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

  • Ana-Check Ref K831463

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

  • Counter-Check Plus Ref K791750

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

  • Crp-Check Ref K831465

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

  • Ebv-Check(Tm) Test Kit (Igg) Ref K871373

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

  • Aso-Check Ref K831464

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

  • Counter Check, H001, H002, H003 Ref K790025

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

  • Counter-Check Plus Normal, High Abn. Ref K791772

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

  • Count-A-Part Plus Ref K841809

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

  • Im-Check Ref K834345

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

  • Ebv/Vca-Check(Tm) Antigen Slides Ref K863408

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

  • Ebv/Ea-Check Tm Test Kit Ref K903612

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

  • Chlamydia-Check(Tm) Direct & Culture Confir. Kit Ref K864128

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

  • Pha-1 Programmable Hematology Analyz Ref K834372

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

  • Picoscale Laborscale, #psl-1 & Analyser, #psa-1 Ref K853036

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

  • Ra-Check Ref K831467

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

  • B Hcg-Check Ref K831468

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

  • Pha-2 Conversion Program For Platelet Analysis Ref K860586

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

  • Ebna-Check(Tm) Test Kit Ref K891542

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

  • Hcg-Check Ref K831466

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

Rows 1-28 of 28

Frequently asked questions

How many devices does Diagnostic Technology, Inc. have in the registry?

The registry currently lists 28 devices for Diagnostic Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Diagnostic Technology, Inc.'s devices?

Among its 28 most recently registered devices, Diagnostic Technology, Inc. has devices listed in FDA 510(k) (28 devices).

What risk classes do Diagnostic Technology, Inc.'s devices fall under?

Among its 28 most recently registered devices, the classes recorded for Diagnostic Technology, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Diagnostic Technology, Inc. in the registry?

The most recently registered devices listed for Diagnostic Technology, Inc. include DIGITAL RADIOGRAPHY SYSTEM, PICOSCALE BLOOD CELL COUNTER, MODEL PS-5, SICKLE-CHECK and LASER-CAL.

Generated automatically from registry data and not verified by a human reviewer.