510(k) K982532 ยท FTL Mesh, Surgical, Polymeric
PARIETEX
| Applicant | Cogent, Washington DC, US |
| Decision | Substantially Equivalent, Jan 20, 1999 |
| Received | Jul 20, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982532
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.