Toshibamedical Systems Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Toshibamedical Systems Corporation - FDA 510(k) Cleared Devices
Recent clearances: Viamo c100 TUS-VC100 Diagnostic Ultrasound System, Aquilion Precision (TSX-304A/2) V8.6 with FIRST 3.0, Vitrea Software Toshiba Package VSTP-001A
80
Total
80
Cleared
0
Denied
Toshibamedical Systems Corporation has 80 FDA 510(k) cleared radiology devices. Based in Tustin, US.
Historical record: 80 cleared submissions from 2004 to 2018.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Toshiba America Medical Systems, In.C as regulatory consultant.
FDA 510(k) Regulatory Record - Toshibamedical Systems Corporation
80 devices
Cleared
Apr 20, 2018
Viamo c100 TUS-VC100 Diagnostic Ultrasound System
Radiology
113d
Cleared
Feb 23, 2018
Aquilion Precision (TSX-304A/2) V8.6 with FIRST 3.0
Radiology
107d
Cleared
Jan 31, 2018
Vitrea Software Toshiba Package VSTP-001A
Radiology
124d
Cleared
Jan 26, 2018
Vantage Galan 3T, V4.6
Radiology
88d
Cleared
Jan 11, 2018
Aplio i900/i800/i700/i600 Diagnostic Ultrasound System, V2.4
Radiology
104d
Cleared
Dec 14, 2017
Infinix-i, INFX-8000V, V7.0
Radiology
85d
Cleared
Dec 12, 2017
Xario 200 Diagnostic Ultrasound System V6.0
Radiology
137d
Cleared
Oct 30, 2017
XIDF-AWS801, Angio Workstation, V7.0
Radiology
59d
Cleared
Jul 21, 2017
Ultimax-i, DREX-UI80 V1.60
Radiology
123d
Cleared
Jul 21, 2017
Vantage Elan 1.5T, V4.0
Radiology
51d
Cleared
Jun 30, 2017
Aquilion ONE (TSX-305A/3) V8.3 with FIRST 2.1
Radiology
162d
Cleared
Jun 08, 2017
Vitrea Software Toshiba Package
Radiology
43d
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