510(k) K080530 ยท GEX Powered Laser Surgical Instrument
MODIFICATION TO CUTERA ER:YSGG LASER HANDPIECE
| Applicant | Cutera, Inc., Brisbane CA, US |
| Decision | Substantially Equivalent, Aug 15, 2008 |
| Received | Feb 26, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K080530
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.