510(k) K130983 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
GENII ARC SMART ARGON PROBE
| Applicant | Genii, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Sep 26, 2013 |
| Received | Apr 9, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130983
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.