510(k) K942152 ยท GEX Powered Laser Surgical Instrument
CANDELA Q-SWITCHED, FREQUENCY DOUBLED ND;YAG LASER SY
| Applicant | Candela Laser Corp., Wayland MA, US |
| Decision | Substantially Equivalent, Jul 25, 1994 |
| Received | May 3, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K942152
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.