510(k) K030539 ยท GEX Powered Laser Surgical Instrument
LASERSMILE
| Applicant | Biolase Technology, Inc., Clemente CA, US |
| Decision | Substantially Equivalent, Oct 10, 2003 |
| Received | Feb 20, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K030539
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.