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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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