The Newman Group, LLC
United StatesFDA applicant, unverified
- Devices
- 2
What The Newman Group, LLC makes
The Newman Group, LLC makes the Babybeat Cordless and Digdop Ultrasound System devices.
These devices are classified as Class II and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Babybeat Cordless Ref K061091
Regimes: 510(k) Registry: 510(k)Digdop Ultrasound System Ref K090465
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does The Newman Group, LLC have in the registry?
The registry currently lists 2 devices for The Newman Group, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list The Newman Group, LLC's devices?
Among its 2 most recently registered devices, The Newman Group, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do The Newman Group, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for The Newman Group, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from The Newman Group, LLC in the registry?
The most recently registered devices listed for The Newman Group, LLC include BABYBEAT CORDLESS and DIGDOP ULTRASOUND SYSTEM.