# Bruel & Kjaer Industri A/S

- Location (FDA's records): Denmark, DK
- FDA decisions: 4 (1984–1992): 4 510(k) clearances
- Product codes: IYO (3), EQL (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 5 (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)
- Teratech Corp.: 1 (https://510kreport.com/company/teratech)
- 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
- K914945: Diagnostic Ultrasound System Type 3535, Modified (1992), cited by 5

## Recent decisions
- K914945: Diagnostic Ultrasound System Type 3535, Modified (Jun 26, 1992)
- K875357: Biopsy Fixation Unit-Type UA 0997 (Jul 1, 1988)
- K852502: Amendment Ultrasound Scanner Type 1842/1846/1849 (Oct 23, 1986)
- K842090: Rhino-Larynx Stroboscope Type 4914 (Jul 18, 1984)

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