510(k) K953412 ยท GEX Powered Laser Surgical Instrument
CANDELA MODEL PLTL-1 LASER SYSTEM
| Applicant | Candela Laser Corp., Washington DC, US |
| Decision | Substantially Equivalent, Oct 24, 1995 |
| Received | Jul 20, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953412
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.