K-number	K895266
Device name	AMBULATORY (HOLTER) RECORDING SYSTEM - MODIFIED
Applicant	Biosensor Corp.
Product code	DSI
Device class	Class II
Decision date	Jan 26, 1990
Decision	Substantially Equivalent
Regulation	870.1025

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View the full FDA submission: accessdata.fda.gov

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AMBULATORY (HOLTER) RECORDING SYSTEM - MODIFIED

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