510(k) K100474 ยท GEX Powered Laser Surgical Instrument
QUICKLASEDUAL+, QUICKLASE810, QUICKLASE810, QUICKLASE980, QUICKLASE980 MODEL: 3W,5W,3W,5W
| Applicant | Quicklase Limited, Riverton UT, US |
| Decision | Substantially Equivalent, Mar 16, 2010 |
| Received | Feb 18, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K100474
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.