K-number	K841083
Device name	QUIKPAGE ARRHYTHMIA REPORT GENERATOR
Applicant	Agilent Technologies
Product code	DSI
Device class	Class II
Decision date	Feb 7, 1985
Decision	Substantially Equivalent
Regulation	870.1025

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View the full FDA submission: accessdata.fda.gov

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QUIKPAGE ARRHYTHMIA REPORT GENERATOR

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