510(k) K020958 ยท GEX Powered Laser Surgical Instrument
CANDELA CBEAM PULSED DYE LASER SYSTEM
| Applicant | Candela Corp., Wayland MA, US |
| Decision | Substantially Equivalent, Jun 21, 2002 |
| Received | Mar 25, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020958
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.