K-number	K110287
Device name	PHILIPS ECG LEADWIRE SET
Applicant	Philips Medical Systems
Product code	DSA
Device class	Class II
Decision date	Feb 15, 2011
Decision	Substantially Equivalent
Regulation	870.2900

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Source

View the full FDA submission: accessdata.fda.gov

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PHILIPS ECG LEADWIRE SET

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