510(k) K062321 ยท GEX Powered Laser Surgical Instrument
SMARTLIPO ND:YAG LASER
| Applicant | Cynosure, Inc., Wesford MA, US |
| Decision | Substantially Equivalent, Oct 31, 2006 |
| Received | Aug 9, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062321
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.