FDA 510(k) Applications Submitted by JEFF BARRETT

FDA 510(k) Number Submission Date Device Name Applicant
K122593 08/24/2012 PRECISION ENDOSCOPIC INFRARED COAGULATOR; MODEL 5100 SINGLE-USE DISPOSABLE MAXI-GUIDE FLEXIBLE LIGHTGUIDE; MODEL 5100-2 OPTIM LLC
K130489 02/25/2013 ELECTRODE, FLEXIBLE SUCTION COAGULATOR OPTIM, LLC.


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