510(k) K231548 ยท GEX Powered Laser Surgical Instrument
Medical Diode Laser, Model S1Pro
| Applicant | Wuhan Pioon Technology Co., Ltd., Wuhan, CN |
| Decision | Substantially Equivalent, Aug 3, 2023 |
| Received | May 30, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231548
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.