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Cdc Anaerobe Blood Agar

by Bd Becton Dickinson Vacutainer Systems Preanalytic

510(k) K803025

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None ongoing

2 closed

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK803025 Date22 Dec 1980ClearedStatusActive

Recalls

2 recalls · FDA

    • Terminated Z-0975-2015 FDA Class II initiated 6 Jun 2014

    A low level of surface and subsurface contamination of Listeria monocytogenes on 9 lots of non-sterile prepared plated media containing sheep blood, typically visible immediately upon removal from the packaging. The contamination is typically observed as 1-3 CFUs per plate when present.

    • Terminated Z-1334-2013 FDA Class II initiated 11 Mar 2013

    Microbiological media may be contaminated with bacteria.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA Product Code
JSG
Device Class
Class I
Regulation
21 CFR Part 866.2300
Advisory Committee
Microbiology
FDA Decision
SESE Substantially Equivalent

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