510(k) K063556 ยท FTM Mesh, Surgical
PERIPATCH ENDO-SLEEVE
| Applicant | Pm Devices, Inc., Richmond, CA |
| Decision | Substantially Equivalent, Mar 20, 2007 |
| Received | Nov 27, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K063556
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.