K-number	K093869
Device name	SE-601 SERIES ELECTROCARDIOGRAPH
Applicant	Edan Instruments, Inc.
Product code	DPS
Device class	Class II
Decision date	Apr 1, 2010
Decision	Substantially Equivalent
Regulation	870.2340

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View the full FDA submission: accessdata.fda.gov

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SE-601 SERIES ELECTROCARDIOGRAPH

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