510(k) K180593 ยท GEX Powered Laser Surgical Instrument
Vbeam Prima Laser System
| Applicant | Syneron-Candela, Wayland MA, US |
| Decision | Substantially Equivalent, Jun 5, 2018 |
| Received | Mar 6, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180593
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.