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
FDA 510(k) Regulatory Record - Aloka Co., Ltd. Radiology ✕
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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