510(k) K181523 ยท GEX Powered Laser Surgical Instrument
Syneron CO2RE System
| Applicant | Syneron-Candela Corp, Wayland MA, US |
| Decision | Substantially Equivalent, Jul 11, 2018 |
| Received | Jun 11, 2018 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K181523
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.