K-number	K083677
Device name	PHYSIOGLOVE FOR USE WITH PHYSIOGLOVE ES1
Applicant	Commwell , Ltd.
Product code	DRX
Device class	Class II
Decision date	Mar 10, 2009
Decision	Substantially Equivalent
Regulation	870.2360

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View the full FDA submission: accessdata.fda.gov

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PHYSIOGLOVE FOR USE WITH PHYSIOGLOVE ES1

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