510(k) K123037 ยท GEX Powered Laser Surgical Instrument
LIGHTSCALPEL
| Applicant | Lightscalpel, LLC, Woodinville WA, US |
| Decision | Substantially Equivalent, Nov 29, 2012 |
| Received | Sep 28, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123037
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.