510(k) K230990 ยท GEX Powered Laser Surgical Instrument
Candela Vbeam Family of Pulsed Dye Lasers (Vbeam Prima, Vbeam Perfecta)
| Applicant | Candela Corporation, Marlborough MA, US |
| Decision | Substantially Equivalent, Jun 1, 2023 |
| Received | Apr 6, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230990
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.