510(k) K855104 ยท GES Blade, Scalpel
ANGIOMED SKIN FASCIA KNIFE
| Applicant | Angiomed U.S., Inc., Anaheim CA, US |
| Decision | Substantially Equivalent, Jan 24, 1986 |
| Received | Dec 23, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K855104
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.