510(k) K933586 ยท DTZ Oxygenator, Cardiopulmonary Bypass
MINIMAX PLUS HOLLOW FIBER OXYGENATOR (WITH OR WITHOUT MEDTRONIC/CARMEDA BIOACTIVE SURFACE
| Applicant | Medtronic Vascular, Anaheim CA, US |
| Decision | Substantially Equivalent, Feb 7, 1994 |
| Received | Jul 26, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933586
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.