Cis Bio International
Country not established
- Devices
- 1
What Cis Bio International makes
Cis Bio International manufactures the CISBIO Renin Radioimmunoassay (RIA) Test, a diagnostic assay designed to measure renin levels in blood samples for clinical evaluation of renin-related conditions.
The CISBIO Renin RIA Test is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance database. The company is based in the United States.
Catalogue
Cisbio Renin Ria Test Ref K062120
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cis Bio International have in the registry?
The registry currently lists 1 device for Cis Bio International. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cis Bio International's devices?
Among its 1 most recently registered device, Cis Bio International has devices listed in FDA 510(k) (1 device).
What risk classes do Cis Bio International's devices fall under?
Among its 1 most recently registered device, the classes recorded for Cis Bio International's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cis Bio International in the registry?
The most recently registered devices listed for Cis Bio International include CISBIO RENIN RIA TEST.