510(k) K962609 ยท LRH Instrument For Auto Reader Of Overnight Microorganism Identification System
GRAM NEGATIVE IDENTIFICATION PLUS CARD
| Applicant | Biomerieux Vitek, Inc., Hazelwood MO, US |
| Decision | Substantially Equivalent, Aug 30, 1996 |
| Received | Jul 3, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962609
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.