510(k) K220053 ยท KGE Forceps, Biopsy, Electric
Diathermic Slitter (FlushKnife) DK2620JI and DK2623JI
| Applicant | Fujifilm Corporation, Ashigara Kami-Gun, JP |
| Decision | Substantially Equivalent, Feb 4, 2022 |
| Received | Jan 6, 2022 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K220053
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.