510(k) K930415 ยท GKG Centrifuge, Hematocrit
MICROHEMATOCRIT ROTOR
| Applicant | Fisher Scientific Co., LLC, Pittsburgh PA, US |
| Decision | Substantially Equivalent, Mar 23, 1993 |
| Received | Jan 26, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K930415
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.