Biim Ultrasound AS is one of 19 FDA 510(k) medical device manufacturers from Norway in the dataset, ranked by real submission volume.
Biim Ultrasound AS - FDA 510(k) Cleared Devices
Recent clearances: Biim Diagnostic Ultrasound System
1
Total
1
Cleared
0
Denied
Biim Ultrasound AS has 1 FDA 510(k) cleared medical devices. Based in Narvik, NO.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Biim Ultrasound AS Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Biim Ultrasound AS
1 devices