Qbc Accutube

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K953340 ↗

FDA Product Code

GKZ

Device Class

Class II

Regulation

21 CFR Part 864.5220

Advisory Committee

Hematology

FDA Decision

SESE Substantially Equivalent

• Bactec(R) 9000TB System

  Class I

  FDA 510(k) K946268 Active Cleared 21 May 1996

• Qbc Accuread System

  Class II

  FDA 510(k) K955504 Active Cleared 5 Feb 1996

• Bactec Lytic/10 Anaerobic/F Culture Vials

  Class I

  FDA 510(k) K954925 Active Cleared 16 Feb 1996

• Bactec Standard/10 Aerobic/F Culture Vials

  Class I

  FDA 510(k) K954921 Active Cleared 16 Feb 1996

• Qbc Accutube

  Class II

  FDA 510(k) K945205 Active Cleared 25 Sep 1995

• Bactec Peds Plus Cluture Vials

  Class I

  FDA 510(k) K954924 Active Cleared 8 Feb 1996

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