Kp Medcure, Inc.
Country not established
- Devices
- 1
What Kp Medcure, Inc. makes
Kp Medcure, Inc. manufactures the CAPERE Thrombectomy System, a device designed for the mechanical removal of blood clots within blood vessels, primarily used in neurovascular and peripheral applications.
The CAPERE Thrombectomy System is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
CAPERE Thrombectomy System Ref K180722
510(k) 510(k)
Frequently asked questions
How many devices does Kp Medcure, Inc. have in the registry?
The registry currently lists 1 device for Kp Medcure, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kp Medcure, Inc.'s devices?
Among its 1 most recently registered device, Kp Medcure, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Kp Medcure, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Kp Medcure, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kp Medcure, Inc. in the registry?
The most recently registered devices listed for Kp Medcure, Inc. include CAPERE Thrombectomy System.