K-number	K171337
Device name	LENSAR Laser System fs 3D (LLS-fs 3D)
Applicant	Lensar, Inc.
Product code	OOE
Device class	Class II
Decision date	Aug 10, 2017
Decision	Substantially Equivalent
Regulation	886.4390

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Source

View the full FDA submission: accessdata.fda.gov

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

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