Visiomed Group SA is one of 282 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Visiomed Group SA - FDA 510(k) Cleared Devices
Recent clearances: Bluetooth blood pressure monitor, THERMOFLASH(TM) INFRARED THERMOMETER
2
Total
2
Cleared
0
Denied
Visiomed Group SA has 2 FDA 510(k) cleared medical devices. Based in Paris, FR.
Historical record: 2 cleared submissions from 2011 to 2018. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Visiomed Group SA Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Underwriters Laboratories, Inc. and Shenzhen Kingyield Technology Co., Ltd..
FDA 510(k) Regulatory Record - Visiomed Group SA
2 devices