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FDA 510(k) Applications Submitted by GAUSS SURGICAL, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K163507
12/14/2016
Triton Sponge System
Gauss Surgical, Inc.
DEN130015
02/04/2013
PIXEL 3 SYSTEM
GAUSS SURGICAL, INC.
K120473
02/16/2012
PIXEL APP
GAUSS SURGICAL, INC.
K121274
04/27/2012
PIXEL APP
GAUSS SURGICAL, INC.
K142801
09/29/2014
Triton Canister System
Gauss Surgical, Inc.
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