510(k) K891230 ยท DTZ Oxygenator, Cardiopulmonary Bypass
MAXIMA* HOLLOW FIBER OXYGENATOR W/FILTERED RESERV.
| Applicant | Medtronic Blood Systems, Inc., Anaheim CA, US |
| Decision | Substantially Equivalent, May 19, 1989 |
| Received | Mar 7, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K891230
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.