FDA 510(k) Applications Submitted by Eiken Chemical Co., Ltd.

FDA 510(k) Number Submission Date Device Name Applicant
K092330 08/04/2009 OC-SENSOR DIANA IFOB TEST EIKEN CHEMICAL CO., LTD.
K191147 04/30/2019 OC-Auto SENSOR io iFOB Test Eiken Chemical Co., Ltd.


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