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Becton Dickinson Diagnostic Instrument Systems

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Devices
13

What Becton Dickinson Diagnostic Instrument Systems makes

The company manufactures automated blood culture systems, including the BACTEC 9000TB and BACTEC 9050 systems, designed for detecting and identifying bacterial and fungal infections in clinical samples. It also produces QBC AccuRead and QBC Accutube systems for blood analysis, as well as culture vials for aerobic, anaerobic, and pediatric bacterial cultures. Additional offerings include fungal growth media and MGIT products for mycobacterial detection.

These devices are regulated under FDA 510(k) clearance, with classifications spanning Class I and Class II. The portfolio is listed in the FDA’s 510(k) registry, and the company operates from the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

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  • Bactec(R) 9000TB System Ref K946268

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

  • Qbc Accuread System Ref K955504

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

  • Bactec Lytic/10 Anaerobic/F Culture Vials Ref K954925

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

  • Bactec Standard/10 Aerobic/F Culture Vials Ref K954921

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

  • Qbc Accutube Ref K945205

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

  • Bactec Peds Plus Cluture Vials Ref K954924

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

  • Qbc Accutube(423406)/Qbc Autoread(424571) Ref K960827

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

  • Bactec Culture Vials, Lytic, Anaerobic Ref K954930

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

  • Qbc Accutube Ref K953340

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

  • Bbl Mgit Products Ref K954932

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

  • Bactec Fungal Medium Ref K954923

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

  • Bactec 9050 System Ref K962210

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

  • Bactec Peds Plus/F Culture Vials Ref K954927

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

Rows 1-13 of 13

Frequently asked questions

How many devices does Becton Dickinson Diagnostic Instrument Systems have in the registry?

The registry currently lists 13 devices for Becton Dickinson Diagnostic Instrument Systems. Devices recorded under merged duplicate company entries are counted once.

Which registries list Becton Dickinson Diagnostic Instrument Systems's devices?

Among its 13 most recently registered devices, Becton Dickinson Diagnostic Instrument Systems has devices listed in FDA 510(k) (13 devices).

What risk classes do Becton Dickinson Diagnostic Instrument Systems's devices fall under?

Among its 13 most recently registered devices, the classes recorded for Becton Dickinson Diagnostic Instrument Systems's devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Becton Dickinson Diagnostic Instrument Systems in the registry?

The most recently registered devices listed for Becton Dickinson Diagnostic Instrument Systems include BACTEC(R) 9000TB SYSTEM, QBC ACCUREAD SYSTEM, BACTEC LYTIC/10 ANAEROBIC/F CULTURE VIALS and BACTEC STANDARD/10 AEROBIC/F CULTURE VIALS.

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