Pediacath, Inc.
Country not established
- Devices
- 1
What Pediacath, Inc. makes
Pediacath, Inc. manufactures the Mongoose Angiographic Catheter, a device designed for pediatric interventional radiology procedures to facilitate vascular imaging and access in small patients.
The Mongoose Angiographic Catheter is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Mongoose Angiographic Catheter Ref K113819
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pediacath, Inc. have in the registry?
The registry currently lists 1 device for Pediacath, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pediacath, Inc.'s devices?
Among its 1 most recently registered device, Pediacath, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Pediacath, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Pediacath, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pediacath, Inc. in the registry?
The most recently registered devices listed for Pediacath, Inc. include MONGOOSE ANGIOGRAPHIC CATHETER.