FDA 510(k) Applications Submitted by ALCON LENSX, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K120732 | 03/09/2012 | LENSSX LASER SYSTEM | ALCON LENSX, INC. |
| K123120 | 10/03/2012 | LENSX LASER SYSTEM | ALCON LENSX, INC. |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact