510(k) K123120 ยท OOE Ophthalmic Femtosecond Laser
LENSX LASER SYSTEM
| Applicant | Alcon Lensx, Inc., Laguna Beach CA, US |
| Decision | Substantially Equivalent, Dec 12, 2012 |
| Received | Oct 3, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123120
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.