510(k) K223778 ยท GEX Powered Laser Surgical Instrument
Diode Laser Hair Removal System (RD-SLD600)
| Applicant | Shanghai Omni Laser Skinology Co., Ltd., Shanghai, CN |
| Decision | Substantially Equivalent, Mar 31, 2023 |
| Received | Dec 16, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223778
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.