510(k) K961803 ยท GKG Centrifuge, Hematocrit
SPUNCRIT (MODEL DRC-40)
| Applicant | Micro Diagnostics Corp., Bethlehem PA, US |
| Decision | Substantially Equivalent, Jul 5, 1996 |
| Received | May 9, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961803
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.