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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