FDA 510(k) Applications Submitted by PRONOSCO A/S

FDA 510(k) Number Submission Date Device Name Applicant
K002500 08/14/2000 X-POSURE SYSTEM VERSION 2 RAD PRONOSCO A/S
K003656 11/27/2000 X-POSURE SYSTEM VERSION 2 MAMMO PRONOSCO A/S


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