Cdc Anaerobe Blood Agar
by Bd Becton Dickinson Vacutainer Systems Preanalytic
510(k) K803025
Active
510(k)
Valid until
No expiry
FDA recalls
None ongoingDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK803025 | Date22 Dec 1980 | StatusActive |
Recalls
-
- Terminated Z-0975-2015
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
Microbiological media may be contaminated with bacteria.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 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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