K-number	K072217
Device name	ECG-1250A SERIES CARDIOFAX S AND ECG-1350A SERIES CARDIOFAX M
Applicant	Nihon Kohden America, Inc.
Product code	DPS
Device class	Class II
Decision date	Aug 30, 2007
Decision	Substantially Equivalent
Regulation	870.2340

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View the full FDA submission: accessdata.fda.gov

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ECG-1250A SERIES CARDIOFAX S AND ECG-1350A SERIES CARDIOFAX M

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