510(k) K920889 ยท DTZ Oxygenator, Cardiopulmonary Bypass
MINIMAX(R)/MAXIMA(R) HOLLOW FIBER OXYGENATORS
| Applicant | Medtronic Vascular, Anaheim CA, US |
| Decision | Substantially Equivalent, Sep 15, 1992 |
| Received | Feb 12, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920889
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.