510(k) K072261 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
FINESSE SYSTEM
| Applicant | Primaeva Medical, Inc., Fremont CA, US |
| Decision | Substantially Equivalent, Dec 26, 2007 |
| Received | Aug 14, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072261
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.