510(k) K033331 ยท GEX Powered Laser Surgical Instrument
CANDELA CBEAM PULSE DYE LASER SYSTEM
| Applicant | Candela Corp., Wayland MA, US |
| Decision | Substantially Equivalent, Jan 16, 2004 |
| Received | Oct 16, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K033331
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.