Cleared Special

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

K152453 · Lensar, Inc. · Ophthalmic

Oct 2015

Decision

48d

Days

Class 2

Risk

About This 510(k) Submission

K152453 is an FDA 510(k) clearance for the LENSAR Laser System - fs 3D (LLS-fs 3D), a Ophthalmic Femtosecond Laser (Class II — Special Controls, product code OOE), submitted by Lensar, Inc. (Orlando, US). The FDA issued a Cleared decision on October 15, 2015, 48 days after receiving the submission on August 28, 2015. This device falls under the Ophthalmic review panel. Regulated under 21 CFR 886.4390.

Submission Details

510(k) Number	K152453 FDA.gov
FDA Decision	Cleared SESE
Date Received	August 28, 2015
Decision Date	October 15, 2015
Days to Decision	48 days
Submission Type	Special
Review Panel	Ophthalmic (OP)
Summary	Summary PDF

Device Classification

Product Code	OOE — Ophthalmic Femtosecond Laser
Device Class	Class II — Special Controls
CFR Regulation	21 CFR 886.4390
Definition	Precise Cutting Or Ablation Of Ocular Tissue, Indicated For The Anterior Capsulotomy During Cataract Surgery.