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FDA 510(k) Applications Submitted by Thomas Bento
FDA 510(k) Number
Submission Date
Device Name
Applicant
K190468
02/26/2019
Nihon Kohden SVM-7200 Series Vital Signs Monitor
Nihon Kohden Corporation
K171765
06/14/2017
Nihon Kohden CO2 Monitor
Nihon Kohden Corporation
K161860
07/06/2016
TG-970P CO2 Sensor Kit
NIHON KOHDEN CORPORATION
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