510(k) K924158 ยท GEX Powered Laser Surgical Instrument
CANDELA LASSER SYSTEMS MODIFIED
| Applicant | Candela Laser Corp., Wayland MA, US |
| Decision | Substantially Equivalent, Jan 15, 1993 |
| Received | Aug 18, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K924158
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.