510(k) K923272 ยท DTZ Oxygenator, Cardiopulmonary Bypass
COBE CMS-HF HOLLOW FIBER MEMBRANE OXYGENATOR
| Applicant | Cobe Laboratories, Inc., Arvada CO, US |
| Decision | Substantially Equivalent, May 11, 1993 |
| Received | Jul 6, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K923272
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.