510(k) K002479 ยท FTL Mesh, Surgical, Polymeric
BIOMESH P1 AND BIOMESH PLUG AND PATCH
| Applicant | Cousin Biotech S.A.R.L, Washington DC, US |
| Decision | Substantially Equivalent, Oct 19, 2000 |
| Received | Aug 11, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K002479
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.