510(k) K092860 ยท GEX Powered Laser Surgical Instrument
LASEMAR 800, 1000, 1500
| Applicant | Eufoton S.R.L., Trieste, IT |
| Decision | Substantially Equivalent, Jul 16, 2010 |
| Received | Sep 17, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092860
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.