510(k) K962641 ยท DTZ Oxygenator, Cardiopulmonary Bypass
MAXIMA FORTE HOLLOW FIBER OXYGENATOR WITH PLASMA RESISTANT FIBER
| Applicant | Medtronic Vascular, Anaheim CA, US |
| Decision | Substantially Equivalent, Dec 16, 1996 |
| Received | Jul 5, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962641
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.