Jerry Mccarty
Country not established
- Devices
- 1
What Jerry Mccarty makes
Jerry McCarty manufactures the HAND-E-BREATH, a manual resuscitation device designed for emergency use in cardiopulmonary resuscitation (CPR).
The device is classified as Class II under FDA regulations and is listed via 510(k) clearance. The manufacturer operates from the United States.
Catalogue
Hand-E-Breath Ref K921339
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Jerry Mccarty have in the registry?
The registry currently lists 1 device for Jerry Mccarty. Devices recorded under merged duplicate company entries are counted once.
Which registries list Jerry Mccarty's devices?
Among its 1 most recently registered device, Jerry Mccarty has devices listed in FDA 510(k) (1 device).
What risk classes do Jerry Mccarty's devices fall under?
Among its 1 most recently registered device, the classes recorded for Jerry Mccarty's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Jerry Mccarty in the registry?
The most recently registered devices listed for Jerry Mccarty include HAND-E-BREATH.