American Radiosurgery, Inc. is one of 20454 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
American Radiosurgery, Inc. - FDA 510(k) Cleared Devices
Recent clearances: EXPLORER 4D TREATMENT PLANNING SYSTEM, EXPLORER 4D TREATMENT PLANNING SYSTEM, ROTATING GAMMA SYSTEM. GAMMA ART-6000
3
Total
3
Cleared
0
Denied
American Radiosurgery, Inc. has 3 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 3 cleared submissions from 2006 to 2010. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by American Radiosurgery, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - American Radiosurgery, Inc.
3 devices