Begley Enterprises, Inc.
Country not established
- Devices
- 1
What Begley Enterprises, Inc. makes
Begley Enterprises, Inc. manufactures the RESUSIKIT, a medical emergency response kit designed for resuscitation procedures.
The RESUSIKIT is classified as a Class I device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Resusikit Ref K861482
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Begley Enterprises, Inc. have in the registry?
The registry currently lists 1 device for Begley Enterprises, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Begley Enterprises, Inc.'s devices?
Among its 1 most recently registered device, Begley Enterprises, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Begley Enterprises, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Begley Enterprises, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Begley Enterprises, Inc. in the registry?
The most recently registered devices listed for Begley Enterprises, Inc. include RESUSIKIT.