K-number	K112844
Device name	REHASTIM 2, REHAMOVE 2
Applicant	Hasomed GmbH
Product code	GZI
Device class	Class II
Decision date	Oct 27, 2011
Decision	Substantially Equivalent
Regulation	882.5810

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View the full FDA submission: accessdata.fda.gov

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REHASTIM 2, REHAMOVE 2

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