Aloka Co., Ltd. is one of 79 FDA 510(k) medical device manufacturers from Japan in the dataset, ranked by real submission volume.
Aloka Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: ALOKA SSD-3500 DIAGNOSTIC ULTRASOUND SYSTEM, ALOKA PROUSOUND F75 DIAGNOSTIC ULTRASOUND SYSTEM, ALOKA PROSOUND ALPHA 6 DIAGNOSTIC ULTRASOUND SYSTEM
39
Total
39
Cleared
0
Denied
Aloka Co., Ltd. has 39 FDA 510(k) cleared radiology devices. Based in Tokyo, JP.
Historical record: 39 cleared submissions from 1982 to 2011.
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 Intertek Testing Services and Tuv Rheinland of North America, Inc..
FDA 510(k) Regulatory Record - Aloka Co., Ltd.
39 devices
Cleared
May 13, 2011
ALOKA SSD-3500 DIAGNOSTIC ULTRASOUND SYSTEM
Radiology
11d
Cleared
Feb 17, 2011
ALOKA PROUSOUND F75 DIAGNOSTIC ULTRASOUND SYSTEM
Radiology
23d
Cleared
Nov 20, 2009
ALOKA PROSOUND ALPHA 6 DIAGNOSTIC ULTRASOUND SYSTEM
Radiology
10d
Cleared
Dec 19, 2008
ALOKA PROUSOUND 2 DIAGNOSTIC ULTRASOUND SYSTEM
Radiology
45d
Cleared
Jul 15, 2008
ULTRASOUND DATA ANALYSIS SYSTEM, MODEL DAS-RS1
Radiology
15d
Cleared
Feb 29, 2008
ALOKA PROSOUND 6 DIAGNOSTIC ULTRASOUND SYSTEM
Radiology
36d
Cleared
Aug 30, 2007
ALOKA SSD-ALPHA 7 ULTRASOUND SYSTEM
Radiology
14d
Cleared
Jan 13, 2006
ALOKA SD-3500 ULTRASOUND SYSTEM
Radiology
4d
Cleared
Nov 30, 2004
ALOKA SSD-ALPHA 10 ULTRASOUND SYSTEM
Radiology
12d
Cleared
Mar 26, 2004
ALOKA MODEL SSD-4000 DIAGNOSTIC ULTRASOUND SYSTEM W/OPTIONAL SONOREAL 3D...
Radiology
7d
Cleared
Oct 29, 2003
ALOKA SSD-5000 V5.0 ULTRASOUND SYSTEM
Radiology
15d
Cleared
Dec 18, 2002
ALOKA SSD-3500 ULTRASOUND SYSTEM
Radiology
15d
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