510(k) K122493 ยท GEX Powered Laser Surgical Instrument
GENESISPLUS
| Applicant | Cutera, Inc., Brisbane CA, US |
| Decision | Substantially Equivalent, May 15, 2013 |
| Received | Aug 16, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122493
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.