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.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact