FDA 510(k) Applications Submitted by OMNITECH SYSTEMS, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K964365 11/01/1996 RESECTOSCOPE CUTTING LOOP ELECTRODE OMNITECH SYSTEMS, INC.
K965093 12/19/1996 OMNITECH RESECTOSCOPE ROLLER ELECTRODE OMNITECH SYSTEMS, INC.
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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