External Counterpulsation Lab
Country not established
- Devices
- 2
What External Counterpulsation Lab makes
The company manufactures automatic external counterpulsation (AECP) devices, designed to improve blood flow and circulation in patients with conditions such as peripheral artery disease or heart failure by applying timed compression to the legs.
These devices are classified as Class II under FDA regulations and are listed in the 510(k) clearance registry. The company operates from the United States.
Catalogue
- 510(k) 510(k)
- 510(k) 510(k)
Frequently asked questions
How many devices does External Counterpulsation Lab have in the registry?
The registry currently lists 2 devices for External Counterpulsation Lab. Devices recorded under merged duplicate company entries are counted once.
Which registries list External Counterpulsation Lab's devices?
Among its 2 most recently registered devices, External Counterpulsation Lab has devices listed in FDA 510(k) (2 devices).
What risk classes do External Counterpulsation Lab's devices fall under?
Among its 2 most recently registered devices, the classes recorded for External Counterpulsation Lab's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from External Counterpulsation Lab in the registry?
The most recently registered devices listed for External Counterpulsation Lab include AECP-A, AUTOMATIC EXTERNAL COUNTERPULSATION DEVICE.