510(k) K120095 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
SIDE EFFECT WITH HAND CONTROLS, HOOK ELECTRODE WITH HAND CONTROLS, 2.3 WEDGE ELECTRODE WITH HAND CONTROLS, S90 WITH HAND
| Applicant | Depuy Mitek, A Johnson & Johnson Company, Raynham MA, US |
| Decision | Substantially Equivalent, Apr 6, 2012 |
| Received | Jan 12, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120095
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.