K-number	K152305
Device name	Nihon Kohden Afib Detection Program QP-039P
Applicant	Nihon Kohden Corporation
Product code	DSI
Device class	Class II
Decision date	Apr 8, 2016
Decision	Substantially Equivalent
Regulation	870.1025

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View the full FDA submission: accessdata.fda.gov

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Nihon Kohden Afib Detection Program QP-039P

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