FDA 510(k) Applications Submitted by J. DAMON KIRK

FDA 510(k) Number Submission Date Device Name Applicant
K060671 03/14/2006 KVUE IGRT TREATMENT TABLE TOP, RT-4551KV, KVUE INSERTS AND ACCESSORIES, VARIOUS WFR/AQUAPLAST CORP.
K032156 07/14/2003 ACCUFIX RADIOLUCENT PELVIS AND BELLY BOARDS, ACCUFIX CANTILEVER HEAD BOARD WITH SHOULDER DEPRESSION, ACCUFIX RADIOLUCENT WFR/AQUAPLAST CORP.


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