510(k) K932252 ยท DTZ Oxygenator, Cardiopulmonary Bypass
AFFINITY HOLLOW FIBER OXYGENATOR
| Applicant | Avecor Cardiovascular, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, Nov 19, 1993 |
| Received | May 26, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932252
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.