LENSAR Laser System - fs 3D (LLS-fs 3D)
K-Number: K173346 · 2018-03-02
Device Summary
Frequently Asked Questions
What is the LENSAR Laser System - fs 3D (LLS-fs 3D)?
LENSAR Laser System - fs 3D (LLS-fs 3D) is a medical device that received FDA 510(k) clearance on 2018-03-02. It is manufactured by Lensar, Inc.. The 510(k) number is K173346.
When was LENSAR Laser System - fs 3D (LLS-fs 3D) approved by the FDA?
LENSAR Laser System - fs 3D (LLS-fs 3D) received FDA 510(k) clearance on 2018-03-02, under approval number K173346.
What company makes LENSAR Laser System - fs 3D (LLS-fs 3D)?
LENSAR Laser System - fs 3D (LLS-fs 3D) is manufactured by Lensar, Inc..
What is the FDA product code for LENSAR Laser System - fs 3D (LLS-fs 3D)?
The FDA product code for LENSAR Laser System - fs 3D (LLS-fs 3D) is OOE.
Related Clinical Trials
Other Devices by Lensar, 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.