510(k) K172077 ยท GEX Powered Laser Surgical Instrument
Cutera enlighten III Laser System
| Applicant | Cutera, Inc., Brisbane CA, US |
| Decision | Substantially Equivalent, Oct 27, 2017 |
| Received | Jul 10, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172077
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.