510(k) K904336 ยท GKF Instrument, Hematocrit, Automated
NEW COBE SATURATION/HEMATOCRIT MONITOR
| Applicant | Cobe Laboratories, Inc., Arvada CO, US |
| Decision | Substantially Equivalent, Dec 27, 1990 |
| Received | Sep 20, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904336
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.