K-number	K051534
Device name	CARDIOLINE AR 600, AR 1200, AR 2100
Applicant	Et Medical Devices Spa
Product code	DPS
Device class	Class II
Decision date	Oct 5, 2005
Decision	Substantially Equivalent
Regulation	870.2340

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View the full FDA submission: accessdata.fda.gov

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CARDIOLINE AR 600, AR 1200, AR 2100

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