510(k) K161186 ยท KGE Forceps, Biopsy, Electric
Fujifilm Diathermic Slitter (FlushKnife), Fujifilm Diathermic Slitter (ClutchCutter)
| Applicant | Fujifilm Medical Systems U.S.A, Inc., Wayne NJ, US |
| Decision | Substantially Equivalent, Jun 29, 2016 |
| Received | Apr 27, 2016 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K161186
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.