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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