510(k) K893678 ยท KRH Ring, Annuloplasty
DURAN FLEXIBLE ANNULOPLASTY RING & OBTURATOR H601H
| Applicant | Medtronic Blood Systems, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Nov 27, 1989 |
| Received | May 16, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K893678
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.