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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