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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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