510(k) K864039 ยท GKF Instrument, Hematocrit, Automated
MICROHEMATOCRIT CENTRIFUGE
| Applicant | Plaza Medical, Inc., Denver CO, US |
| Decision | Substantially Equivalent, Oct 29, 1986 |
| Received | Oct 16, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K864039
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.