K-number	K190034
Device name	REMY Medical Therapy Laser System
Applicant	Footdocprenur, LLC
Product code	PDZ
Device class	Class II
Decision date	May 15, 2019
Decision	Substantially Equivalent
Regulation	878.4810

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Source

View the full FDA submission: accessdata.fda.gov

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REMY Medical Therapy Laser System

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