510(k) K101817 ยท GEX Powered Laser Surgical Instrument
LIGHTWALKER AT, MODEL M021-5AF/1, LIGHTWALKER DT, MODEL M021-5AF/2, LIGHTWALKER ST-E, MODEL M002-6A/2, LIGHTWALKER ST-N
| Applicant | Fotona D.D., Ljubljana, SI |
| Decision | Substantially Equivalent, Nov 22, 2010 |
| Received | Jun 30, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101817
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.