510(k) K840172 ยท FTL Mesh, Surgical, Polymeric
VENTRAL WALL DEFECT REDUCT SILO
| Applicant | American Heyer Schulte, Mchenry IL, US |
| Decision | Substantially Equivalent, Jun 27, 1984 |
| Received | Jan 17, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K840172
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.