510(k) K183428 ยท KGE Forceps, Biopsy, Electric
Avulsion Forceps
| Applicant | STERIS Corporation, Mentor OH, US |
| Decision | Substantially Equivalent, Apr 16, 2019 |
| Received | Dec 11, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K183428
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.