K-number	K840274
Device name	CARDIOFAX ECG 6543
Applicant	Nihon Kohden America, Inc.
Product code	DRS
Device class	Class II
Decision date	Apr 17, 1984
Decision	Substantially Equivalent
Regulation	870.2850

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View the full FDA submission: accessdata.fda.gov

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CARDIOFAX ECG 6543

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