Great Lakes Intl.
Country not established
- Devices
- 1
What Great Lakes Intl. makes
Great Lakes Intl. manufactures the BAKTERIETTE-VI-PAK, a device designed for microbiological testing, specifically for culturing and identifying bacteria in clinical or laboratory settings.
The BAKTERIETTE-VI-PAK is classified as a Class I medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Bakteriette-Vi-Pak Ref K840719
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Great Lakes Intl. have in the registry?
The registry currently lists 1 device for Great Lakes Intl.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Great Lakes Intl.'s devices?
Among its 1 most recently registered device, Great Lakes Intl. has devices listed in FDA 510(k) (1 device).
What risk classes do Great Lakes Intl.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Great Lakes Intl.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Great Lakes Intl. in the registry?
The most recently registered devices listed for Great Lakes Intl. include BAKTERIETTE-VI-PAK.