Hitachi Medical Systems America, Inc. - FDA 510(k) Cleared Devices
100
Total
100
Cleared
0
Denied
Hitachi Medical Systems America, Inc. has 100 FDA 510(k) cleared radiology devices. Based in Twinsburg, US.
Historical record: 100 cleared submissions from 1991 to 2017.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
100 devices
Cleared
Mar 03, 2017
HITACHI Supria Whole-body X-ray CT System Phase 3
Radiology
77d
Cleared
Sep 16, 2016
TRILLIUM Oval Head Coil 32
Radiology
51d
Cleared
Aug 17, 2016
SUPRIA w/guideShot Option
Radiology
54d
Cleared
May 20, 2016
Trillium Oval V 5.1 MRI System
Radiology
119d
Cleared
Mar 31, 2016
ECHELON Oval V 5.1 MRI System
Radiology
111d
Cleared
Oct 30, 2015
SCENARIA Phase 3 Whole-body X-ray CT System
Radiology
235d
Cleared
Sep 30, 2015
Supria Whole-body X-ray CT System
Radiology
208d
Cleared
Jul 29, 2015
ECHELON Oval V 5.0 MRI System
Radiology
104d
Cleared
Mar 06, 2015
Sirius Starmobile tiara
Radiology
81d
Cleared
Mar 02, 2015
TRILLIUM Oval MR System
Radiology
160d
Cleared
Mar 29, 2013
SCENARIA PHASE 2 WHOLE-BODY X-RAY CT SYSTEM
Radiology
136d
Cleared
May 03, 2012
GUIDESHOT OPTION, SCENARIA WHOLE-BODY X-RAY CT SYSTEM
Radiology
171d
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