510(k) K122829 ยท HQC Unit, Phacofragmentation
LENSAR LASER SYSTEM - FS 3D FOR CORNEAL INCISIONS
| Applicant | Lensar, Inc., Orlando FL, US |
| Decision | Substantially Equivalent, Dec 3, 2012 |
| Received | Sep 17, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122829
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.