510(k) K070392 ยท GEX Powered Laser Surgical Instrument
MOSAIC LASER SYSTEM
| Applicant | Lutronic Corporation, North Reading MA, US |
| Decision | Substantially Equivalent, Jul 13, 2007 |
| Received | Feb 9, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070392
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.