510(k) K032810 ยท KRH Ring, Annuloplasty
DURAN BAND (MODEL H607H), DURAN RING (MODEL 610R), DURAN BAND (MODEL 610B), DURAN ANCORE RING (MODEL 620R), DURAN ANCORE
| Applicant | Medtronic Heart Valves, Minneapolis MN, US |
| Decision | Substantially Equivalent, Dec 5, 2003 |
| Received | Sep 9, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K032810
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.