Accuray Incorporated is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Accuray Incorporated - FDA 510(k) Cleared Devices
Recent clearances: Radixact Treatment Delivery System, Accuray Precision Treatment Planning System, ClearRT Helical kVCT for the Radixact Treatment Delivery System
21
Total
21
Cleared
0
Denied
Accuray Incorporated has 21 FDA 510(k) cleared radiology devices. Based in Sunnyvale, US.
Last cleared in 2023. Active since 2004.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Accuray Incorporated
21 devices
Cleared
Jun 23, 2023
Radixact Treatment Delivery System
Radiology
259d
Cleared
Sep 30, 2021
Accuray Precision Treatment Planning System
Radiology
28d
Cleared
Dec 18, 2020
ClearRT Helical kVCT for the Radixact Treatment Delivery System
Radiology
116d
Cleared
Nov 23, 2018
Motion Tracking and Compensation Feature for the Radixact Treatment Delivery...
Radiology
58d
Cleared
Jul 25, 2017
TomoTherapy Treatment Delivery System with iDMS
Radiology
35d
Cleared
Jun 08, 2017
Accuray Precision Treatment Planning System
Radiology
57d
Cleared
Jun 24, 2016
Precision Treatment Planning System
Radiology
63d
Cleared
Jun 24, 2016
iDMS Data Management System
Radiology
63d
Cleared
Jun 24, 2016
Radixact Treatment Delivery System
Radiology
63d
Cleared
Sep 28, 2015
Onrad Treatment System
Radiology
28d
Cleared
Jul 01, 2015
CyberKnife M6 FI Sytem, CyberKnife M6 FM System, CyberKnife M6 FIM System
Radiology
91d
Cleared
Apr 14, 2015
Delivery Analysis
Radiology
152d