510(k) K151229 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
ABC D-FLEX PROBE
| Applicant | Conmed Corporation, Utica NY, US |
| Decision | Substantially Equivalent, Jun 2, 2016 |
| Received | May 7, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151229
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.