510(k) K861285 ยท GFD Dermatome
SKIN MESH DEVICE
| Applicant | Precision Modified Devices, Salt Lake City UT, US |
| Decision | Substantially Equivalent, Apr 17, 1986 |
| Received | Apr 7, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K861285
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.