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FDA 510(k) Applications Submitted by JON D BARRETT
FDA 510(k) Number
Submission Date
Device Name
Applicant
K050454
02/22/2005
OMNITECH FULGURATING ELECTRODE
OMNITECH SYSTEMS, INC.
K981463
04/23/1998
OMNITECH RESECTOSCOPE ROLLER ELECTRODE
OMNITECH SYSTEMS, INC.
K981464
04/23/1998
OMNITECH RESECTOSCOPE CUTTING LOOP ELECTRODE
OMNITECH SYSTEMS, INC.
K151976
07/16/2015
Omnitech HF Resection Electrodes, Omnitech HF Vaporization Electrode
OMNITECH SYSTEMS, INC.
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