510(k) K061366 ยท GEX Powered Laser Surgical Instrument
DENLASER 800 PLUS
| Applicant | CAO Group, Inc., Sandy UT, US |
| Decision | Substantially Equivalent, Jul 10, 2006 |
| Received | May 16, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061366
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.