510(k) K934811 ยท GEX Powered Laser Surgical Instrument
PLTL-1 & PLDL-1 510NM PULSED DYE LASERS
| Applicant | Candela Laser Corp., Wayland MA, US |
| Decision | Substantially Equivalent, Sep 1, 1994 |
| Received | Oct 7, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K934811
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.