FDA 510(k) Applications Submitted by ANDY DORAISWAMY

FDA 510(k) Number Submission Date Device Name Applicant
K210885 03/25/2021 Dayspring Koya Medical, Inc.
DEN160030 07/07/2016 Oculeve Intranasal Tear Neurostimulator Device OCULEVE, INC.
K193288 11/27/2019 Koya Ripple Koya, Inc.


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