510(k) K181602 ยท GEX Powered Laser Surgical Instrument
Pioneer Elite Diode Laser
| Applicant | CAO Group, Inc., West Jordan UT, US |
| Decision | Substantially Equivalent, Sep 10, 2019 |
| Received | Jun 19, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181602
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.