510(k) K094052 ยท OOE Ophthalmic Femtosecond Laser
LENSX 550 LASER SYSTEM. MODEL 550
| Applicant | Lensx Lasers, Inc., Laguna Beach CA, US |
| Decision | Substantially Equivalent, Apr 23, 2010 |
| Received | Dec 31, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K094052
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.