510(k) K063072 ยท GEX Powered Laser Surgical Instrument
CANDELA FAMILY OF Q-SWITCHED ALEXANDRITE LASER (ALEXLAZR) SYSTEMS: 532 AND 1064 ND:YAG HANDPIECE ACCESSORIES
| Applicant | Candela Corp., Wayland MA, US |
| Decision | Substantially Equivalent, Dec 20, 2006 |
| Received | Oct 6, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K063072
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.