R4, LLC
Country not established
- Devices
- 1
What R4, LLC makes
R4, LLC makes the R4 ACERT Ultrasound Reporting System, a software-based medical device used for generating and managing ultrasound examination reports.
The R4 ACERT Ultrasound Reporting System is classified as a Class II device and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
R4 Acert Ultrasound Reporting System Ref K101898
510(k) 510(k)
Frequently asked questions
How many devices does R4, LLC have in the registry?
The registry currently lists 1 device for R4, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list R4, LLC's devices?
Among its 1 most recently registered device, R4, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do R4, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for R4, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from R4, LLC in the registry?
The most recently registered devices listed for R4, LLC include R4 ACERT ULTRASOUND REPORTING SYSTEM.