Patient Data Systems
Country not established
- Devices
- 1
What Patient Data Systems makes
Patient Data Systems manufactures the CVA, a medical device designed for stroke patient monitoring and data collection to support clinical assessment and care planning.
The CVA is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Patient Data Systems Cva Ref K852175
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Patient Data Systems have in the registry?
The registry currently lists 1 device for Patient Data Systems. Devices recorded under merged duplicate company entries are counted once.
Which registries list Patient Data Systems's devices?
Among its 1 most recently registered device, Patient Data Systems has devices listed in FDA 510(k) (1 device).
What risk classes do Patient Data Systems's devices fall under?
Among its 1 most recently registered device, the classes recorded for Patient Data Systems's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Patient Data Systems in the registry?
The most recently registered devices listed for Patient Data Systems include PATIENT DATA SYSTEMS CVA.