K-number	K860212
Device name	CARDIOFAX ECG-6353
Applicant	Nihon Kohden America, Inc.
Product code	DPS
Device class	Class II
Decision date	Apr 17, 1986
Decision	Substantially Equivalent
Regulation	870.2340

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View the full FDA submission: accessdata.fda.gov

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CARDIOFAX ECG-6353

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