Medical Device Manufacturer · DK , Denmark

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

1 submissions · 1 cleared · Since 1986

Total

Cleared

Denied

A/S Bruel & Kjaer has 1 FDA 510(k) cleared medical devices. Based in Denmark, DK.

Historical record: 1 cleared submissions from 1986 to 1986. Primary specialty: Ear, Nose, Throat.

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

A/S Bruel & Kjaer is one of 44 FDA 510(k) medical device manufacturers from Denmark in the dataset, ranked by real submission volume.

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

1 devices

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