Biomira Diagnostics, Inc.
CanadaFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Visuwell Syphilis Antibody Ref K932453
Regimes: 510(k) Registry: 510(k)Visuwell Reagin Ii Ref K952802
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Biomira Diagnostics, Inc. have in the registry?
The registry currently lists 2 devices for Biomira Diagnostics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Biomira Diagnostics, Inc.'s devices?
Among its 2 most recently registered devices, Biomira Diagnostics, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Biomira Diagnostics, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Biomira Diagnostics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Biomira Diagnostics, Inc. in the registry?
The most recently registered devices listed for Biomira Diagnostics, Inc. include VISUWELL SYPHILIS ANTIBODY and VISUWELL REAGIN II.