Hitachi Aloka Medical,Ltd. (Hitachi Aloka Medical is one of 18926 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hitachi Aloka Medical,Ltd. (Hitachi Aloka Medical - FDA 510(k) Cleare...
Recent clearances: ARIETTA 60/ARIETTAS60/ARIETTAV60, ARIETTA 70/ARIETTA S70/ARIETTA V70 DIAGNOSTIC ULTRASOUND SCANNER, PROUSOUND ALPHA 7 VER. 6.0 DIAGNOSTIC ULTRASOUND SYSTEM MODEL: PROSOUND ALPHA 7 VER. 6.0
3
Total
3
Cleared
0
Denied
Hitachi Aloka Medical,Ltd. (Hitachi Aloka Medical has 3 FDA 510(k) cleared medical devices. Based in Wallingford, US.
Historical record: 3 cleared submissions from 2013 to 2014. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Hitachi Aloka Medical,Ltd. (Hitachi Aloka Medical Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv Rheinland of North America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Hitachi Aloka Medical,Ltd. (Hitachi Aloka Medical
3 devices