510(k) K163551 ยท OOE Ophthalmic Femtosecond Laser
LenSx Laser System
| Applicant | Alcon Laboratories, Inc., Lake Forest CA, US |
| Decision | Substantially Equivalent, Feb 3, 2017 |
| Received | Dec 19, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K163551
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.