Great Lakes Bioscience
Country not established
- Devices
- 1
What Great Lakes Bioscience makes
Great Lakes Bioscience manufactures the GLB Varicella-Zoster Virus Fluorescent diagnostic test.
The company is based in the United States, and its product is classified as a Class II medical device listed in the FDA 510(k) registry.
Catalogue
Glb Varicella-Zoster Virus Fluorescent Ref K842096
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Great Lakes Bioscience have in the registry?
The registry currently lists 1 device for Great Lakes Bioscience. Devices recorded under merged duplicate company entries are counted once.
Which registries list Great Lakes Bioscience's devices?
Among its 1 most recently registered device, Great Lakes Bioscience has devices listed in FDA 510(k) (1 device).
What risk classes do Great Lakes Bioscience's devices fall under?
Among its 1 most recently registered device, the classes recorded for Great Lakes Bioscience's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Great Lakes Bioscience in the registry?
The most recently registered devices listed for Great Lakes Bioscience include GLB VARICELLA-ZOSTER VIRUS FLUORESCENT.