Toshiba America Medical Systems, In.C is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Toshiba America Medical Systems, In.C - FDA 510(k) Cleared Devices
Recent clearances: VANTAGE ELAN, KALARE, APLIO ARTIDA, V3.2
146
Total
146
Cleared
0
Denied
Toshiba America Medical Systems, In.C has 146 FDA 510(k) cleared radiology devices. Based in Tustin, US.
Historical record: 146 cleared submissions from 1989 to 2014.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Regulatory Technology Services, LLC, Tuv Product Service, Inc. and Tuv America, Inc..
FDA 510(k) Regulatory Record - Toshiba America Medical Systems, In.C
146 devices
Cleared
Sep 19, 2014
VANTAGE ELAN
Radiology
108d
Cleared
Jun 13, 2014
KALARE
Radiology
206d
Cleared
May 23, 2014
APLIO ARTIDA, V3.2
Radiology
60d
Cleared
Nov 12, 2013
INFINIX ANGIO WORKSTATION W/DTS SOFTWARE
Radiology
127d
Cleared
Jul 23, 2013
ULTRAEXTEND USWS-900A V2.1 AND V3.1
Radiology
33d
Cleared
Feb 13, 2013
DOSE TRACKING SYSTEM MODEL XIDF-DTS801
Radiology
134d
Cleared
Dec 13, 2012
VANTAGE TITAN WITH HELIOS GRADIENT MODEL MRT-1504/US
Radiology
108d
Cleared
Oct 09, 2012
ULTRAEXTEND FX, ULTRASOUND WORKSTATION PACKAGE
Radiology
183d
Cleared
Oct 09, 2012
RADREX-I, SW V4.00 MODEL DRAD-3000E
Radiology
22d
Cleared
Sep 21, 2012
AQUILION ONE VISION, V4.90
Radiology
66d
Cleared
Apr 10, 2012
AQUILION CXL
Radiology
187d
Cleared
Jan 26, 2012
AQUILION PRIME
Radiology
381d
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