510(k) K914602 ยท KRH Ring, Annuloplasty
DURAN FLEX ANNULOPLASTY RING/OBTUR H601H, MODIFIED
| Applicant | The Heart Valve Div. Medtronic Cardiovascular Surg, Minneapolis MN, US |
| Decision | Substantially Equivalent, Nov 22, 1991 |
| Received | Oct 15, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K914602
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.