K-number	K874716
Device name	PULSOR, THERAPEUTIC VIBRATOR
Applicant	Gmg Enterprises, Inc.
Product code	ISA
Device class	Class I
Decision date	Feb 11, 1988
Decision	Substantially Equivalent
Regulation	890.5660

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View the full FDA submission: accessdata.fda.gov

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PULSOR, THERAPEUTIC VIBRATOR

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