Toshiba Medical Systems Corporation, Japan is one of 15062 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Toshiba Medical Systems Corporation, Japan - FDA 510(k) Cleared Devic...
Recent clearances: Vantage Titan 3T, MRT-3010/A7, M-Power GX, SURESUBTRACTION LUNG, OCTAVE SPEEDER HEAD
9
Total
9
Cleared
0
Denied
Toshiba Medical Systems Corporation, Japan has 9 FDA 510(k) cleared medical devices. Based in Tustin, US.
Historical record: 9 cleared submissions from 2011 to 2017. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Toshiba Medical Systems Corporation, Japan 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 - Toshiba Medical Systems Corporation, Japan
9 devices
Cleared
Nov 17, 2017
Vantage Titan 3T, MRT-3010/A7, M-Power GX
Radiology
57d
Cleared
Sep 05, 2014
SURESUBTRACTION LUNG
Radiology
311d
Cleared
Aug 17, 2012
OCTAVE SPEEDER HEAD
Radiology
49d
Cleared
Aug 17, 2012
OCTAVE SPEEDER SPINE
Radiology
49d
Cleared
Jun 22, 2012
APLIO ARTIDA DIAGNOSTIC ULTRASOUND SYSTEM
Radiology
23d
Cleared
Jun 13, 2012
AQUILION PREMIUM
Radiology
111d
Cleared
Aug 05, 2011
INFINIX CF-I/SP AND INFINIX VF-I/SP MODEL INFX-8000V
Radiology
17d
Cleared
Aug 02, 2011
VANTAGE TITAN 3T
Radiology
336d
Cleared
Jan 12, 2011
APLIO XG DIAGNOSTIC ULTRASOUND SYSTEM
Radiology
30d