K-number	K091791
Device name	PROVANT SYSTEM, MODEL 4201
Applicant	Regenesis Biomedical, Inc.
Product code	ILX
Device class	Class II
Decision date	Apr 7, 2010
Decision	Substantially Equivalent
Regulation	890.5290

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View the full FDA submission: accessdata.fda.gov

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PROVANT SYSTEM, MODEL 4201

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