510(k) K081324 ยท GEX Powered Laser Surgical Instrument
CANDELA FAMILY OF Q-SWITCHED ALEXANDRITE LASERS
| Applicant | Candela Corp., Wayland MA, US |
| Decision | Substantially Equivalent, Jun 17, 2008 |
| Received | May 12, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K081324
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.