Sonoscanner is one of 247 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Sonoscanner - FDA 510(k) Cleared Devices
Recent clearances: T-Lite, U-Lite EXP
2
Total
2
Cleared
0
Denied
Sonoscanner has 2 FDA 510(k) cleared medical devices. Based in Ivry Sur Seine, FR.
Historical record: 2 cleared submissions from 2017 to 2020. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Sonoscanner Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Smith Associates and Smith Assoicates.
FDA 510(k) Regulatory Record - Sonoscanner
2 devices