Renalpro Medical, Inc.
Country not established
- Devices
- 1
What Renalpro Medical, Inc. makes
Renalpro Medical, Inc. manufactures the AortaSTAT Occlusion Device, a medical device designed for vascular occlusion during interventional procedures.
The device falls under FDA Class II regulation and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
AortaSTAT Occlusion Device Ref K210602
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Renalpro Medical, Inc. have in the registry?
The registry currently lists 1 device for Renalpro Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Renalpro Medical, Inc.'s devices?
Among its 1 most recently registered device, Renalpro Medical, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Renalpro Medical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Renalpro Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Renalpro Medical, Inc. in the registry?
The most recently registered devices listed for Renalpro Medical, Inc. include AortaSTAT Occlusion Device.