510(k) K964967 ยท DTZ Oxygenator, Cardiopulmonary Bypass
BIOCOR 200 HIGH PERFORMANCEOXYGENATOR
| Applicant | Minntech Corp., Minneapolis MN, US |
| Decision | Substantially Equivalent, Mar 6, 1997 |
| Received | Dec 10, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K964967
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.