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FDA 510(k)

LENSAR Laser System - fs 3D (LLS-fs 3D)

K-Number: K173346 · 2018-03-02

ApplicantLensar, Inc.
Decision Date2018-03-02
Product CodeOOE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

LENSAR Laser System - fs 3D (LLS-fs 3D) is a medical device manufactured by Lensar, Inc.. It received FDA 510(k) clearance on 2018-03-02 under approval number K173346. The device is classified under product code OOE. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.