LenSx Laser System
K-Number: K173660 · 2018-03-27
Device Summary
Frequently Asked Questions
What is the LenSx Laser System?
LenSx Laser System is a medical device that received FDA 510(k) clearance on 2018-03-27. It is manufactured by Alcon Laboratories, Inc.. The 510(k) number is K173660.
When was LenSx Laser System approved by the FDA?
LenSx Laser System received FDA 510(k) clearance on 2018-03-27, under approval number K173660.
What company makes LenSx Laser System?
LenSx Laser System is manufactured by Alcon Laboratories, Inc..
What is the FDA product code for LenSx Laser System?
The FDA product code for LenSx Laser System is OOE.
Related Clinical Trials
Other Devices by Alcon Laboratories, Inc.
Related Devices (Code: OOE)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.