Autogenic Systems
Country not established
- Devices
- 1
What Autogenic Systems makes
Autogenic Systems manufactures centrifugal analyzers designed for automated blood and fluid sample processing in clinical or point-of-care settings. These devices separate components like plasma or cells via high-speed rotation, enabling rapid diagnostic testing or sample preparation.
The company’s centrifugal analyzers fall under FDA Class I regulatory classification, requiring 510(k) clearance for market authorisation. The devices are listed in the FDA’s 510(k) database, and the manufacturer operates from the United States.
Catalogue
Analyzer, Automed Centrifugal Ref K781900
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Autogenic Systems have in the registry?
The registry currently lists 1 device for Autogenic Systems. Devices recorded under merged duplicate company entries are counted once.
Which registries list Autogenic Systems's devices?
Among its 1 most recently registered device, Autogenic Systems has devices listed in FDA 510(k) (1 device).
What risk classes do Autogenic Systems's devices fall under?
Among its 1 most recently registered device, the classes recorded for Autogenic Systems's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Autogenic Systems in the registry?
The most recently registered devices listed for Autogenic Systems include ANALYZER, AUTOMED CENTRIFUGAL.