K-number	K830013
Device name	EPI CARDIA SYS. - AMBULATORY MONITOR
Applicant	Medicomp, Inc.
Product code	DSI
Device class	Class II
Decision date	Feb 28, 1983
Decision	Substantially Equivalent
Regulation	870.1025

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View the full FDA submission: accessdata.fda.gov

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EPI CARDIA SYS. - AMBULATORY MONITOR

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