Bruel & Kjaer Instruments, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 4
What Bruel & Kjaer Instruments, Inc. makes
Bruel & Kjaer Instruments, Inc. manufactures diagnostic ultrasound scanners, including handheld and real-time imaging devices, as well as anesthetic gas monitors for patient safety. The company also produces vibrometry systems for assessing mechanical vibrations in medical or industrial applications.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Scanner Type 1846 Ref K827380
510(k) 510(k)Real Time Ultrasound Scanner 1849 Ref K827409
510(k) 510(k)Anesthetic Gas Monitor Ref K890446
510(k) 510(k)Vibrometry System Ref K901881
510(k) 510(k)
Frequently asked questions
How many devices does Bruel & Kjaer Instruments, Inc. have in the registry?
The registry currently lists 4 devices for Bruel & Kjaer Instruments, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bruel & Kjaer Instruments, Inc.'s devices?
Among its 4 most recently registered devices, Bruel & Kjaer Instruments, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Bruel & Kjaer Instruments, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Bruel & Kjaer Instruments, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bruel & Kjaer Instruments, Inc. in the registry?
The most recently registered devices listed for Bruel & Kjaer Instruments, Inc. include SCANNER TYPE 1846, REAL TIME ULTRASOUND SCANNER 1849, ANESTHETIC GAS MONITOR and VIBROMETRY SYSTEM.