510(k) K040835 ยท FTM Mesh, Surgical
PERIPATCH SHEET, MODELS 1.5P8, 1.5P16, 4P4, 4P6, 6P8 AND 10P16
| Applicant | Pm Devices, Inc., Richmond, Bc, CA |
| Decision | Substantially Equivalent, Jun 15, 2004 |
| Received | Mar 31, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K040835
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.