Cardiassist Corp.
Country not established
- Devices
- 1
What Cardiassist Corp. makes
Cardiassist Corp. manufactures the CardiAssist External Counterpulsation device, designed for temporary circulatory support by augmenting blood flow during diastole.
The company’s portfolio is regulated under FDA Class II devices and requires 510(k) clearance. The device is listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Cardiassist External Counterpulsation Ref K792430
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cardiassist Corp. have in the registry?
The registry currently lists 1 device for Cardiassist Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cardiassist Corp.'s devices?
Among its 1 most recently registered device, Cardiassist Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Cardiassist Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Cardiassist Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cardiassist Corp. in the registry?
The most recently registered devices listed for Cardiassist Corp. include CARDIASSIST EXTERNAL COUNTERPULSATION.