510(k) K915441 ยท GKF Instrument, Hematocrit, Automated
MARATHON 13K/H MICROHEMATOCRIT CENTRIFUGE
| Applicant | Fisher Scientific Co., LLC, Indiana PA, US |
| Decision | Substantially Equivalent, Jan 8, 1992 |
| Received | Dec 4, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K915441
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.