Universal H.R. System, Inc.
Country not established
- Devices
- 1
What Universal H.R. System, Inc. makes
Universal H.R. System, Inc. makes the EPI 2 device.
The EPI 2 is a Class I medical device listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
Epi 2 Ref K935706
510(k) 510(k)
Frequently asked questions
How many devices does Universal H.R. System, Inc. have in the registry?
The registry currently lists 1 device for Universal H.R. System, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Universal H.R. System, Inc.'s devices?
Among its 1 most recently registered device, Universal H.R. System, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Universal H.R. System, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Universal H.R. System, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Universal H.R. System, Inc. in the registry?
The most recently registered devices listed for Universal H.R. System, Inc. include EPI 2.