FDA 510(k), K153707, Nihon Kohden Vital Sign Telemeter

FDA 510(k), K153707, Nihon Kohden Vital Sign Telemeter

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510(K) Number: K153707
Device Name: Nihon Kohden Vital Sign Telemeter
Manufacturer: NIHON KOHDEN CORPORATION
Device Classification Name: monitor, physiological, patient(with arrhythmia detection or alarms)
Regulation Number: 870.1025
Classification Product Code: MHX
Date Received: 12/23/2015
Decision Date: 09/02/2016
Regulation Medical Specialty: Cardiovascular

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