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FDA 510(k) Applications Submitted by HITACHI ALOKA MEDICAL,LTD. (HITACHI ALOKA MEDICAL
FDA 510(k) Number
Submission Date
Device Name
Applicant
K140443
02/21/2014
ARIETTA 60/ARIETTAS60/ARIETTAV60
HITACHI ALOKA MEDICAL,LTD. (HITACHI ALOKA MEDICAL
K134016
12/30/2013
ARIETTA 70/ARIETTA S70/ARIETTA V70 DIAGNOSTIC ULTRASOUND SCANNER
HITACHI ALOKA MEDICAL,LTD. (HITACHI ALOKA MEDICAL
K122537
08/20/2012
PROUSOUND ALPHA 7 VER. 6.0 DIAGNOSTIC ULTRASOUND SYSTEM MODEL: PROSOUND ALPHA 7 VER. 6.0
HITACHI ALOKA MEDICAL,LTD. (HITACHI ALOKA MEDICAL
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