510(k) K792646 ยท KRH Ring, Annuloplasty
AMP DIRECT VASCULAR MONITORING SYSTEM
| Applicant | American Medical Products, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 11, 1980 |
| Received | Dec 21, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K792646
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.