510(k) K221312 ยท GEX Powered Laser Surgical Instrument
Diode Laser Hair Removal Device
| Applicant | Guangzhou Chuang Zao Mei Technology Co., Ltd., Guangzhou, CN |
| Decision | Substantially Equivalent, Jun 29, 2022 |
| Received | May 5, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K221312
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.