510(k) K141476 ยท OOE Ophthalmic Femtosecond Laser
WAVELIGHT FS200 LASER SYSTEM
| Applicant | Alcon Research, Ltd. Dba Alcon Laboratories, Inc., Fort Worth TX, US |
| Decision | Substantially Equivalent, Sep 30, 2014 |
| Received | Jun 4, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K141476
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.