510(k) K052354 ยท GEX Powered Laser Surgical Instrument
OCULASE MD
| Applicant | Biolase Technology, Inc., Clemente CA, US |
| Decision | Substantially Equivalent, Jul 5, 2006 |
| Received | Aug 29, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K052354
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.