510(k) K961810 ยท FTM Mesh, Surgical
SUPPLE PERI-GUARD PERICARDIUM
| Applicant | Bio-Vascular, Inc., St. Paul MN, US |
| Decision | Substantially Equivalent, Jun 13, 1996 |
| Received | May 10, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961810
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.