FDA 510(k), K010949, 2010 PLUS HOLTER FOR WINDOWS

FDA 510(k), K010949, 2010 PLUS HOLTER FOR WINDOWS

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510(K) Number: K010949
Device Name: 2010 PLUS HOLTER FOR WINDOWS
Manufacturer: AGILENT TECHNOLOGIES
Device Classification Name: electrocardiograph, ambulatory, with analysis algorithm
Regulation Number: 870.2800
Classification Product Code: MLO
Date Received: 03/29/2001
Decision Date: 09/28/2001
Regulation Medical Specialty: Cardiovascular

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