510(k) K941473 ยท DTZ Oxygenator, Cardiopulmonary Bypass
MAXIMA PLUS HOLLOW FIBER OXYGENATOR
| Applicant | Medtronic Vascular, Anaheim CA, US |
| Decision | Substantially Equivalent, Jun 21, 1995 |
| Received | Mar 28, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K941473
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.