510(k) K955795 ยท GKG Centrifuge, Hematocrit
MULTI-CENTRIFUGE
| Applicant | Novonx, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Mar 29, 1996 |
| Received | Dec 22, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K955795
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.