510(k) K182924 ยท GEX Powered Laser Surgical Instrument
Diode Laser Treatment System
| Applicant | Weifang KM Electronics Co., Ltd., Weifang, CN |
| Decision | Substantially Equivalent, Apr 15, 2019 |
| Received | Oct 19, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182924
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.