510(k) K240644 ยท GEX Powered Laser Surgical Instrument
Medical Diode Laser (S1Pro)
| Applicant | Wuhan Pioon Technology Co., Ltd., Wuhan, CN |
| Decision | Substantially Equivalent, Jun 10, 2024 |
| Received | Mar 7, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K240644
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.