Hitachi Aloka Medical America, Inc. is one of 18480 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hitachi Aloka Medical America, Inc. - FDA 510(k) Cleared Devices
Recent clearances: UST-5550-R, HI VISION ASCENDUS, HV ASCENDUS, ASCENDUS, Intra-operative Ultrasound Transducer, PROSOUND ALPHA 7 Diagnostic Ultrasound System, ARIETTA 70 Diagnostic Ultrasound System
3
Total
3
Cleared
0
Denied
Hitachi Aloka Medical America, Inc. has 3 FDA 510(k) cleared medical devices. Based in Wallingford, US.
Historical record: 3 cleared submissions from 2014 to 2016. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Hitachi Aloka Medical America, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Hitachi Aloka Medical America, Inc.
3 devices