Medical Device Manufacturer · SE , Solna

Philips Digital Mammography Sweden AB - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2012
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Philips Digital Mammography Sweden AB Radiology ✕
3 devices
1-3 of 3
Cleared Dec 13, 2013
MICRODOSE SI
K130704 · MUE
Radiology · 273d
Cleared Feb 01, 2013
MICRODOSE SI
K123995 · MUE
Radiology · 37d
Cleared Apr 19, 2012
PHILIPS MICRODOSE
K120255 · MUE
Radiology · 83d
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