510(k) K171916 ยท KGE Forceps, Biopsy, Electric
Single Use Hot Biopsy Forceps FD-231
| Applicant | Olympus Medical Systems Corp., Hachioji-Shi, JP |
| Decision | Substantially Equivalent, Oct 13, 2017 |
| Received | Jun 26, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171916
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.