K-number	K063142
Device name	MANUAL PD-IO; POWERED PD-IO
Applicant	Vidacare Corporation
Product code	FMI
Device class	Class II
Decision date	Dec 8, 2006
Decision	Substantially Equivalent
Regulation	880.5570

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View the full FDA submission: accessdata.fda.gov

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MANUAL PD-IO; POWERED PD-IO

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