Iodp SA is one of 25752 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Iodp SA - FDA 510(k) Cleared Devices
Recent clearances: MODEL I0-3DUIMS 3D ULTRASOUND MANAGEMENT SYSTEM
1
Total
1
Cleared
0
Denied
Iodp SA has 1 FDA 510(k) cleared medical devices. Based in Deer Field, US.
Historical record: 1 cleared submissions from 2001 to 2001. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Iodp SA Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Iodp SA
1 devices