Emergency Products and Research
Country not established
- Devices
- 1
What Emergency Products and Research makes
Emergency Products and Research manufactures the PEDI-SPIDER STRAP, a device designed for securing pediatric patients during transport or medical procedures.
The PEDI-SPIDER STRAP is classified as a Class I medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Pedi-Spider Strap Ref K061721
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Emergency Products and Research have in the registry?
The registry currently lists 1 device for Emergency Products and Research. Devices recorded under merged duplicate company entries are counted once.
Which registries list Emergency Products and Research's devices?
Among its 1 most recently registered device, Emergency Products and Research has devices listed in FDA 510(k) (1 device).
What risk classes do Emergency Products and Research's devices fall under?
Among its 1 most recently registered device, the classes recorded for Emergency Products and Research's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Emergency Products and Research in the registry?
The most recently registered devices listed for Emergency Products and Research include PEDI-SPIDER STRAP.