510(k) K915825 ยท GKF Instrument, Hematocrit, Automated
MARATHON 6K GENERAL-PURPOSE CENTRIFUGE
| Applicant | Fisher Scientific Co., LLC, Indiana PA, US |
| Decision | Substantially Equivalent, Mar 11, 1992 |
| Received | Dec 30, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K915825
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.