510(k) K173660 ยท OOE Ophthalmic Femtosecond Laser
LenSx Laser System
| Applicant | Alcon Laboratories, Inc., Lake Forest CA, US |
| Decision | Substantially Equivalent, Mar 27, 2018 |
| Received | Nov 29, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173660
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.