Sonoscanner Sarl is one of 274 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Sonoscanner Sarl - FDA 510(k) Cleared Devices
Recent clearances: U-Lite PRO, U-Lite
2
Total
2
Cleared
0
Denied
Sonoscanner Sarl has 2 FDA 510(k) cleared medical devices. Based in Paris, FR.
Latest FDA clearance: Jan 2024. Active since 2015. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Sonoscanner Sarl Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Ferguson Medical International Device Consultants, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Sonoscanner Sarl
2 devices