Isoray, Inc. is one of 18984 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Isoray, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CESITRX, (LIQUID CESIUM-131 SOLUTION) FOR USE WITH GLIASITE RTS, CESIUM-131 STRAND, STRAND PRELOAD, PRELOAD, S-CARTRIDGE, LAWRENCE CSERION, MODEL CS-1
3
Total
3
Cleared
0
Denied
Isoray, Inc. has 3 FDA 510(k) cleared medical devices. Based in Richland, US.
Historical record: 3 cleared submissions from 2003 to 2013. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Isoray, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Isoray, Inc.
3 devices