Alltek Filtration, Inc.
Country not established
- Devices
- 1
What Alltek Filtration, Inc. makes
Alltek Filtration, Inc. manufactures the Q.C. TESTER, a device designed for quality control testing in filtration systems, ensuring compliance with performance standards.
The Q.C. TESTER is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Q.C. Tester Ref K830836
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Alltek Filtration, Inc. have in the registry?
The registry currently lists 1 device for Alltek Filtration, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Alltek Filtration, Inc.'s devices?
Among its 1 most recently registered device, Alltek Filtration, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Alltek Filtration, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Alltek Filtration, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Alltek Filtration, Inc. in the registry?
The most recently registered devices listed for Alltek Filtration, Inc. include Q.C. TESTER.