Krueger Laboratories
Country not established
- Devices
- 1
What Krueger Laboratories makes
Krueger Laboratories manufactures the AcoustiQ listening device, a specialized auditory tool designed for targeted sound amplification and transmission in clinical or diagnostic settings.
The AcoustiQ listening device is classified as a Class II medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Acoustiq Listening Device Ref K904755
510(k) 510(k)
Frequently asked questions
How many devices does Krueger Laboratories have in the registry?
The registry currently lists 1 device for Krueger Laboratories. Devices recorded under merged duplicate company entries are counted once.
Which registries list Krueger Laboratories's devices?
Among its 1 most recently registered device, Krueger Laboratories has devices listed in FDA 510(k) (1 device).
What risk classes do Krueger Laboratories's devices fall under?
Among its 1 most recently registered device, the classes recorded for Krueger Laboratories's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Krueger Laboratories in the registry?
The most recently registered devices listed for Krueger Laboratories include ACOUSTIQ LISTENING DEVICE.