510(k) K781059 ยท GKF Instrument, Hematocrit, Automated
CUTTER/COMPUR MINI CENTRIFUGE
| Applicant | Cutter Laboratories, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 14, 1978 |
| Received | Jun 26, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K781059
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.