510(k) K830993 ยท GFD Dermatome
AMPLIGREFFE
| Applicant | Prothia USA, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, May 3, 1983 |
| Received | Mar 29, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K830993
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.