Hitachi Medical Corp. is one of 129 FDA 510(k) medical device manufacturers from Japan in the dataset, ranked by real submission volume.
Hitachi Medical Corp. - FDA 510(k) Cleared Devices
Recent clearances: OASIS CTL COIL, OD FLEXIBLE BODY COIL (L AND XL), AND RAPID FOOT COIL, MODIFICATION TO EUB-5500 DIAGNOSTIC ULTRASOUND SCANNER, EUB-6500 DIAGNOSTIC ULTRASOUND SCANNER
11
Total
11
Cleared
0
Denied
Hitachi Medical Corp. has 11 FDA 510(k) cleared radiology devices. Based in Tokyo, JP.
Historical record: 11 cleared submissions from 1982 to 2008.
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 - Hitachi Medical Corp.
11 devices
Cleared
Jan 18, 2008
OASIS CTL COIL, OD FLEXIBLE BODY COIL (L AND XL), AND RAPID FOOT COIL
Radiology
56d
Cleared
Nov 22, 2006
MODIFICATION TO EUB-5500 DIAGNOSTIC ULTRASOUND SCANNER
Radiology
166d
Cleared
Dec 09, 2005
EUB-6500 DIAGNOSTIC ULTRASOUND SCANNER
Radiology
17d
Cleared
Oct 12, 2004
ETG-4000 OPTICAL TOPOGRAPHY SYSTEM
Anesthesiology
28d
Cleared
Feb 11, 2002
MODIFICATION TO: EUB-8500 DIAGNOSTIC ULTRASOUND SCANNER
Radiology
94d
Cleared
Feb 06, 2002
MODIFICATION TO: EUB-6500 DIAGNOSTIC ULTRASOUND SCANNER
Radiology
89d
Cleared
Aug 10, 2001
MODIFICATIONS TO EUB-525 DIAGNOSTIC ULTRASOUND SCANNER
Radiology
24d
Cleared
May 30, 2001
EUB-6000 DIAGNOSTIC ULTRASOUND SCANNER SP-711 SONOPROBE SYSTEM
Radiology
36d
Cleared
Jun 03, 1994
EUB-555
Radiology
541d
Cleared
Apr 15, 1991
TRANSDUCERS, EUP-C318/V33/F334/CC331/B31/032T
Radiology
90d
Cleared
Jul 13, 1982
MODEL LS 3000 LINEAR SCANNER
Radiology
84d