510(k) K951085 ยท GFD Dermatome
PADGETT AIR DERMATOME, MODEL A
| Applicant | Padgett Instruments, Inc., Kansas City MO, US |
| Decision | Substantially Equivalent, May 15, 1995 |
| Received | Mar 9, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K951085
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.