Hitachi Healthcare Americas Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hitachi Healthcare Americas Corporation - FDA 510(k) Cleared Devices
Recent clearances: ARIETTA 65, ALOKA ARIETTA 850, ECHELON OVAL V6.0A MRI System
5
Total
5
Cleared
0
Denied
Hitachi Healthcare Americas Corporation has 5 FDA 510(k) cleared medical devices. Based in Twinsburg, US.
Historical record: 5 cleared submissions from 2017 to 2018. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Hitachi Healthcare Americas Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Hitachi Healthcare Americas Corporation
5 devices