FDA 510(k) Applications Submitted by HITACHI ALOKA MEDICAL, LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K122341 08/02/2012 PROSOUND F37 DIAGNOSTIC ULTRASOUND SYSTEM, MODEL: PROSOUND F37 HITACHI ALOKA MEDICAL, LTD.
K123828 12/12/2012 PROSOUND F75 DIAGNOSTIC ULTRASOUND SYSTEM HITACHI ALOKA MEDICAL, LTD.
K130308 02/07/2013 NOBLUS ULTRASOUND DIAGNOSTIC SYSTEM HITACHI ALOKA MEDICAL, LTD.
K140639 03/12/2014 PROSOUND F75 DIAGNOSTIC ULTRASOUND SYSTEM HITACHI ALOKA MEDICAL, LTD.
K140854 04/03/2014 INTRA-OPERATIVE ULTRASOUND TRANSDUCER HITACHI ALOKA MEDICAL, LTD.
K142368 08/25/2014 NOBLUS DIAGNOSTIC ULTRASOUND SCANNER HITACHI ALOKA MEDICAL, LTD.


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