510(k) K123483 ยท GEX Powered Laser Surgical Instrument
DIODE LASER
| Applicant | BEIJING SYNTECH LASER CO., LTD., Shanghai, CN |
| Decision | Substantially Equivalent, Apr 21, 2013 |
| Received | Nov 13, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123483
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.