510(k) K113500 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
CANADY VIEIRA HYBRID PLASMA SCALPEL
| Applicant | Us Medical Innovations, LLC, Lakeland FL, US |
| Decision | Substantially Equivalent, Dec 9, 2011 |
| Received | Nov 25, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K113500
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.