K-number	K873680
Device name	MODEL 6000FD AMBULATORY ECG ANALYSIS SYSTEM
Applicant	Oxford Medilog, Inc.
Product code	DSI
Device class	Class II
Decision date	Nov 23, 1987
Decision	Substantially Equivalent
Regulation	870.1025

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View the full FDA submission: accessdata.fda.gov

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MODEL 6000FD AMBULATORY ECG ANALYSIS SYSTEM

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