Qualiformed Sarl is one of 287 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Qualiformed Sarl - FDA 510(k) Cleared Devices
Recent clearances: LINACwatch, LinacView
1
Total
1
Cleared
0
Denied
Qualiformed Sarl has 1 FDA 510(k) cleared medical devices. Based in La Roche Sur Yon, FR.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Qualiformed Sarl Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Speek TO Market, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Qualiformed Sarl
1 devices