# Bruel & Kjaer

- Location (FDA's records): Naerum 2850, DK
- FDA decisions: 4 (1991–1993): 4 510(k) clearances
- Product codes: CBQ (1), LNH (1), IYN (1), CCK (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 4 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Perception, Inc.: 1 (https://510kreport.com/company/perception)
- CIVCO Medical Instruments Co., Inc.: 1 (https://510kreport.com/company/civco-medical-instruments)
- Pgk, Inc.: 1 (https://510kreport.com/company/pgk)
- Barzell-Whitmore Maroon Bells, Inc.: 1 (https://510kreport.com/company/barzell-whitmore-maroon-bells)

## Its most-cited devices
- K905198: Diagnostic Ultrasound System Type 3535 (1991), cited by 4

## Recent decisions
- K925484: Carbon Dioxide & Oxygen Monitor Type 1308 (Jun 22, 1993)
- K914295: Anesthetic Gas Monitor Type 1304, Modified (Apr 10, 1992)
- K905198: Diagnostic Ultrasound System Type 3535 (Aug 28, 1991)
- K911348: Rigid Endoscope (Jun 21, 1991)

Source page: https://510kreport.com/company/bruel-kjaer