510(k) K993671 ยท GEX Powered Laser Surgical Instrument
CANDELA SCLERO LONG PULSE DYE LASER
| Applicant | Candela Corp., Wayland MA, US |
| Decision | Substantially Equivalent, Jan 24, 2000 |
| Received | Nov 1, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K993671
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.