K-number	K880336
Device name	MOBILIMB HAND C.P.M. UNIT
Applicant	Toronto Medical Corp.
Product code	JFA
Device class	Class I
Decision date	Feb 16, 1988
Decision	Substantially Equivalent
Regulation	890.5410

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View the full FDA submission: accessdata.fda.gov

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MOBILIMB HAND C.P.M. UNIT

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