510(k) K830059 ยท JTC Device, Microtiter Diluting/Dispensing
MUELLER HINTON W/50% SHEEP BLOOD
| Applicant | bioMerieux, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 9, 1983 |
| Received | Jan 11, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K830059
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.