K-number	K063484
Device name	PATIENT DATA HANDLER & DEVICES (PDH&D)
Applicant	Intermed Advisors, Inc.
Product code	DRG
Device class	Class II
Decision date	Dec 22, 2006
Decision	Substantially Equivalent
Regulation	870.2910

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Source

View the full FDA submission: accessdata.fda.gov

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PATIENT DATA HANDLER & DEVICES (PDH&D)

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