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FDA 510(k) Applications Submitted by Tom Bento
FDA 510(k) Number
Submission Date
Device Name
Applicant
K171124
04/17/2017
Nihon Kohden Wireless Input Unit WEE-1200
Nihon Kohden Corporation
K151080
04/22/2015
Nihon Kohden CSM 1901 Bedside Monitor
Nihon Kohden
K152305
08/14/2015
Nihon Kohden Afib Detection Program QP-039P
NIHON KOHDEN CORPORATION
K163459
12/09/2016
Nihon Kohden Vital Sign Telemeter
Nihon Kohden Corporation
K183529
12/19/2018
AE-120A EEG Head Set
Nihon Kohden Corporation
K153707
12/23/2015
Nihon Kohden Vital Sign Telemeter
NIHON KOHDEN CORPORATION
K163644
12/23/2016
Nihon Kohden QP-160AK EEG Trend Program
Nihon Kohden Corporation
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