510(k) K112567 ยท FTL Mesh, Surgical, Polymeric
BIOMERIX ASSURE
| Applicant | Biomerix Corporation, Fremont CA, US |
| Decision | Substantially Equivalent, Dec 23, 2011 |
| Received | Sep 2, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K112567
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.