510(k) K994260 ยท GEX Powered Laser Surgical Instrument
CANDELA GENTLELASE GL DERMATOLOGICAL LASER
| Applicant | Candela Corp., Wayland MA, US |
| Decision | Substantially Equivalent, May 26, 2000 |
| Received | Dec 17, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K994260
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.