510(k) K123310 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
FINESSE 3RD GENERATION (MODELS FINESSE+ AND FINESSEII+)
| Applicant | Utah Medical Products, Inc., Midvale UT, US |
| Decision | Substantially Equivalent, Jan 23, 2013 |
| Received | Oct 25, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123310
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.