510(k) K063800 ยท GEX Powered Laser Surgical Instrument
CANDELA FLUORESCENT PULSED LIGHT SYSTEM
| Applicant | Candela Corp., Wayland MA, US |
| Decision | Substantially Equivalent, Feb 5, 2007 |
| Received | Dec 22, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K063800
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.