FDA 510(k) Applications Submitted by BRIAN J EDWARDS

FDA 510(k) Number Submission Date Device Name Applicant
K050046 01/10/2005 REHABILICARE IF 3 WAVE INTERFERENTIAL STIMULATOR SYSTEM, MODEL 7110S COMPEX TECHNOLOGIES, INC.
K121203 04/20/2012 BOSTON KERATOPROSTHESIS OR BOSTON KPRO MASSACHUSETTS EYE & EAR INFIRMARY
K982220 06/24/1998 MODEL 2872 BIPOLAR LEAD ADAPTOR KIT MEDTRONIC VASCULAR
K132444 08/06/2013 ATAMA SYSTEM MONTERIS MEDICAL


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