510(k) K131059 ยท GEX Powered Laser Surgical Instrument
PIONEER ELITE DIODE LASER
| Applicant | CAO Group, Inc., West Jordan UT, US |
| Decision | Substantially Equivalent, Sep 13, 2013 |
| Received | Apr 16, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131059
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.