FDA 510(k) Applications Submitted by PHILIPS DIGITAL MAMMOGRAPHY SWEDEN AB

FDA 510(k) Number Submission Date Device Name Applicant
K120255 01/27/2012 PHILIPS MICRODOSE PHILIPS DIGITAL MAMMOGRAPHY SWEDEN AB
K130704 03/15/2013 MICRODOSE SI PHILIPS DIGITAL MAMMOGRAPHY SWEDEN AB
K123995 12/26/2012 MICRODOSE SI PHILIPS DIGITAL MAMMOGRAPHY SWEDEN AB


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