Torval Corp.
Country not established
- Devices
- 1
What Torval Corp. makes
Torval Corp. manufactures the SERI-SEP, a medical device designed for sterile separation of biological samples or fluids in clinical or laboratory settings.
The SERI-SEP is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Seri-Sep Ref K770107
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Torval Corp. have in the registry?
The registry currently lists 1 device for Torval Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Torval Corp.'s devices?
Among its 1 most recently registered device, Torval Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Torval Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Torval Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Torval Corp. in the registry?
The most recently registered devices listed for Torval Corp. include SERI-SEP.