FDA 510(k) Applications for Medical Device Product Code "FEH"
(Electrode, Flexible Suction Coagulator)

FDA 510(k) Number Applicant Device Name Decision Date
K122593 OPTIM LLC PRECISION ENDOSCOPIC INFRARED COAGULATOR; MODEL 5100 SINGLE-USE DISPOSABLE MAXI-GUIDE FLEXIBLE LIGHTGUIDE; MODEL 5100-2 09/13/2012
K130489 OPTIM, LLC. ELECTRODE, FLEXIBLE SUCTION COAGULATOR 04/19/2013


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