510(k) K790356 ยท DTZ Oxygenator, Cardiopulmonary Bypass
OXYGENATOR, COBE CATALOG #42-220
| Applicant | Cobe Laboratories, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 9, 1979 |
| Received | Feb 22, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K790356
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.