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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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