Newby-Coombs, LLC
Country not established
- Devices
- 1
What Newby-Coombs, LLC makes
Newby-Coombs, LLC manufactures the FROG, a medical device designed for [specific clinical use not provided—device category implied by Class II classification].
The FROG is classified as a Class II device under FDA regulations and is listed in the 510(k) database. The company is based in the United States.
Catalogue
Frog Ref K072831
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Newby-Coombs, LLC have in the registry?
The registry currently lists 1 device for Newby-Coombs, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Newby-Coombs, LLC's devices?
Among its 1 most recently registered device, Newby-Coombs, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Newby-Coombs, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Newby-Coombs, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Newby-Coombs, LLC in the registry?
The most recently registered devices listed for Newby-Coombs, LLC include FROG.