Philips Digital Mammography Sweden AB

Philips Digital Mammography Sweden AB holds 3 FDA 510(k) medical device clearances, first cleared 2012, most recent 2013.

Top product codes for Philips Digital Mammography Sweden AB

MUE — Radiology3 devices

Recent clearances by Philips Digital Mammography Sweden AB

K130704 — MICRODOSE SICode MUE·2013-12-13
K123995 — MICRODOSE SICode MUE·2013-02-01
K120255 — PHILIPS MICRODOSECode MUE·2012-04-19

Data sourced from openFDA. This site is unofficial and independent of the FDA.