Pixmeo Sarl is one of 24649 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
1
Total
1
Cleared
0
Denied
Pixmeo Sarl has 1 FDA 510(k) cleared medical devices. Based in Denton, US.
Historical record: 1 cleared submissions from 2010 to 2010. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Pixmeo Sarl Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Pixmeo Sarl
1 devices