510(k) K021180 ยท GEX Powered Laser Surgical Instrument
CANDELA VBEAM PULSED DYE LASER SYSTEM
| Applicant | Candela Corp., Wayland MA, US |
| Decision | Substantially Equivalent, Jul 2, 2002 |
| Received | Apr 15, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K021180
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.