510(k) K082586 ยท GEX Powered Laser Surgical Instrument
LIGHTWAVE PROFESSIONAL DELUXE
| Applicant | Lightwave Technologies, LLC, Great Neck NY, US |
| Decision | Substantially Equivalent, Jan 4, 2010 |
| Received | Sep 8, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082586
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.