510(k) K133945 ยท GEX Powered Laser Surgical Instrument
CUTERA PICOSECOND LASER SYSTEM
| Applicant | Cutera, Inc., Brisbane CA, US |
| Decision | Substantially Equivalent, Aug 11, 2014 |
| Received | Dec 23, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133945
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.