K-number	K020456
Device name	EASI 12 LEAD ALGORITHM
Applicant	Philips Medical Systems
Product code	DRW
Device class	Class II
Decision date	Jul 9, 2002
Decision	Substantially Equivalent
Regulation	870.2350

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View the full FDA submission: accessdata.fda.gov

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EASI 12 LEAD ALGORITHM

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