Sopro - Acteon Group is one of 18408 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sopro - Acteon Group - FDA 510(k) Cleared Devices
Recent clearances: S698 Symbioz flow, SOPIX, PSPIX 2 scanner, Imaging Plate Size 0 for PSPIX2 scanner, Imaging Plate Size 1 for PSPIX2 scanner, Imaging Plate Size 2 for PSPIX2 scanner, Imaging Plate Size 3 for PSPIX2 scanner
4
Total
4
Cleared
0
Denied
Sopro - Acteon Group has 4 FDA 510(k) cleared medical devices. Based in Mt. Laurel, US.
Historical record: 4 cleared submissions from 2014 to 2016. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Sopro - Acteon Group Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Acteon, Inc. and Satelec - Acteon Group.
FDA 510(k) Regulatory Record - Sopro - Acteon Group
4 devices