510(k) K151474 ยท KGE Forceps, Biopsy, Electric
Fujifilm Diathermic Slitter (FlushKnife), Diathermic Slitter (ClutchCutter)
| Applicant | Fujifilm Medical System U.S.A., Inc., Wayne NJ, US |
| Decision | Substantially Equivalent, Feb 18, 2016 |
| Received | Jun 1, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151474
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.