K-number	K202537
Device name	ALTMS Magnetic Stimulation Therapy System
Applicant	Remed Co., Ltd.
Product code	OBP
Device class	Class II
Decision date	Nov 26, 2021
Decision	Substantially Equivalent
Regulation	882.5805

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Source

View the full FDA submission: accessdata.fda.gov

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ALTMS Magnetic Stimulation Therapy System

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