510(k) K921989 ยท GHH Fibrin Split Products
FDP - SLIDEX DIRECT
| Applicant | Biomerieux Vitek, Inc., Hazelwood MO, US |
| Decision | Substantially Equivalent, Nov 3, 1993 |
| Received | Apr 28, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K921989
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.