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FDA 510(k) Applications Submitted by Artie Kaushik
FDA 510(k) Number
Submission Date
Device Name
Applicant
K160338
02/08/2016
Triton System
GAUSS SURGICAL INC.
K091733
06/11/2009
VASOVIEW 6 PRO ENDOSCOPIC VESSEL HARVESTING SYSTEM, MODEL VH-2500
MAQUET CARDIOVASCULAR, LLC
K163507
12/14/2016
Triton Sponge System
Gauss Surgical, Inc.
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