The Hilrad Co.
Country not established
- Devices
- 1
What The Hilrad Co. makes
The Hilrad Co. manufactures the STERI-VERS, a device designed for sterilization purposes, likely within a medical or industrial context.
STERI-VERS is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Steri-Vers Ref K810311
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does The Hilrad Co. have in the registry?
The registry currently lists 1 device for The Hilrad Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list The Hilrad Co.'s devices?
Among its 1 most recently registered device, The Hilrad Co. has devices listed in FDA 510(k) (1 device).
What risk classes do The Hilrad Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for The Hilrad Co.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from The Hilrad Co. in the registry?
The most recently registered devices listed for The Hilrad Co. include STERI-VERS.