North American Rescue Products, Inc.
Country not established
- Devices
- 1
What North American Rescue Products, Inc. makes
North American Rescue Products, Inc. makes the Junctional Emergency Treatment Tool Model 30-0088, a medical device designed for emergency hemorrhage control in junctional areas of the body.
This device is classified as Class II and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does North American Rescue Products, Inc. have in the registry?
The registry currently lists 1 device for North American Rescue Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list North American Rescue Products, Inc.'s devices?
Among its 1 most recently registered device, North American Rescue Products, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do North American Rescue Products, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for North American Rescue Products, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from North American Rescue Products, Inc. in the registry?
The most recently registered devices listed for North American Rescue Products, Inc. include JUNCTIONAL EMERGENCY TREATMENT TOOL MODEL 30-0088.