Virion (U.S.), Inc.
United StatesFDA applicant, unverified
- Devices
- 5
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Epstein-Barr Virus Combi Test, Ebv Combi Test Ref K933251
Regimes: 510(k) Registry: 510(k)Toxoplasma Gondii Ref K864981
Regimes: 510(k) Registry: 510(k)Coxsackie Virus B1-B6 Cf Antigens Ref K921618
Regimes: 510(k) Registry: 510(k)P.I.V. Complement-Fixation (C.F.) Antigen Ref K905385
Regimes: 510(k) Registry: 510(k)Mumps Complement-Fixation (C.F.) Antigen Ref K905306
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Virion (U.S.), Inc. have in the registry?
The registry currently lists 5 devices for Virion (U.S.), Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Virion (U.S.), Inc.'s devices?
Among its 5 most recently registered devices, Virion (U.S.), Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Virion (U.S.), Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Virion (U.S.), Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Virion (U.S.), Inc. in the registry?
The most recently registered devices listed for Virion (U.S.), Inc. include EPSTEIN-BARR VIRUS COMBI TEST, EBV COMBI TEST, TOXOPLASMA GONDII, COXSACKIE VIRUS B1-B6 CF ANTIGENS and P.I.V. COMPLEMENT-FIXATION (C.F.) ANTIGEN.