510(k) K041923 ยท FTM Mesh, Surgical
BIOBLANKET
| Applicant | Kensey Nash Corp., Exton PA, US |
| Decision | Substantially Equivalent, Sep 8, 2004 |
| Received | Jul 16, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K041923
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.