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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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