510(k) K120732 ยท HQC Unit, Phacofragmentation
LENSSX LASER SYSTEM
| Applicant | Alcon Lensx, Inc., Laguna Beach CA, US |
| Decision | Substantially Equivalent, Sep 6, 2012 |
| Received | Mar 9, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120732
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Apr 14, 2016 | Alcon Research, Ltd. LenSx Laser System. Indicated for use in patients undergoing cataract surgery and refractive surgery. Terminated |
OOE | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.