Knox Laboratories
Country not established
- Devices
- 1
What Knox Laboratories makes
Knox Laboratories manufactures endoscopic deodorant devices, designed to reduce odor during endoscopic procedures by neutralizing or masking odors within the gastrointestinal tract.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company operates from the United States.
Catalogue
Code 17-Endoscope Deodorant Ref K840208
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Knox Laboratories have in the registry?
The registry currently lists 1 device for Knox Laboratories. Devices recorded under merged duplicate company entries are counted once.
Which registries list Knox Laboratories's devices?
Among its 1 most recently registered device, Knox Laboratories has devices listed in FDA 510(k) (1 device).
What risk classes do Knox Laboratories's devices fall under?
Among its 1 most recently registered device, the classes recorded for Knox Laboratories's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Knox Laboratories in the registry?
The most recently registered devices listed for Knox Laboratories include CODE 17-ENDOSCOPE DEODORANT.