Bruel & Kjaer
DenmarkFDA 510(k) applicant, unverified
- Devices
- 4
Catalogue
Rigid Endoscope Ref K911348
510(k) 510(k)Carbon Dioxide & Oxygen Monitor Type 1308 Ref K925484
510(k) 510(k)Anesthetic Gas Monitor Type 1304, Modified Ref K914295
510(k) 510(k)Diagnostic Ultrasound System Type 3535 Ref K905198
510(k) 510(k)
Frequently asked questions
How many devices does Bruel & Kjaer have in the registry?
The registry currently lists 4 devices for Bruel & Kjaer. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bruel & Kjaer's devices?
Among its 4 most recently registered devices, Bruel & Kjaer has devices listed in FDA 510(k) (4 devices).
What risk classes do Bruel & Kjaer's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Bruel & Kjaer's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bruel & Kjaer in the registry?
The most recently registered devices listed for Bruel & Kjaer include RIGID ENDOSCOPE, CARBON DIOXIDE & OXYGEN MONITOR TYPE 1308, ANESTHETIC GAS MONITOR TYPE 1304, MODIFIED and DIAGNOSTIC ULTRASOUND SYSTEM TYPE 3535.