Elekta, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Elekta, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Monaco RTP System, MOSAIQ Oncology Information System, Monaco RTP System
4
Total
4
Cleared
0
Denied
Elekta, Inc. has 4 FDA 510(k) cleared medical devices. Based in Norcross, US.
Historical record: 4 cleared submissions from 2005 to 2019. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Elekta, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Elekta, Inc.
4 devices