Nuclear Assoc., Div. Inovision LP is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nuclear Assoc., Div. Inovision LP - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Nuclear Assoc., Div. Inovision LP has 1 FDA 510(k) cleared medical devices. Based in Carle Place, US.
Historical record: 1 cleared submissions from 2001 to 2001. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Nuclear Assoc., Div. Inovision LP Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Nuclear Assoc., Div. Inovision LP
1 devices