Medical Device Manufacturer · US , Walker , MI

Bruel & Kjaer Industri A/S - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1984

Total

Cleared

Denied

Bruel & Kjaer Industri A/S has 4 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 4 cleared submissions from 1984 to 1992. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Bruel & Kjaer Industri A/S Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Bruel & Kjaer Industri A/S

4 devices

1-4 of 4