Granbio, Inc.
United StatesFDA applicant, unverified
- Devices
- 7
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Ebna Acif Assay Kit Ref K871298
Regimes: 510(k) Registry: 510(k)(Eia) For Igm Antibody To Ebv Vca In Human Serum Ref K901840
Regimes: 510(k) Registry: 510(k)Indirect Immunofluorescent Antibody Assay Ref K881617
Regimes: 510(k) Registry: 510(k)Ebv Vca Igm Antibody Assay Kit Ref K864604
Regimes: 510(k) Registry: 510(k)Eia For Igg Antibody To Ebv Vca In Human Serum Ref K901156
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Ebna Enzyme Immunoassay Kit Ref K951822
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Granbio, Inc. have in the registry?
The registry currently lists 7 devices for Granbio, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Granbio, Inc.'s devices?
Among its 7 most recently registered devices, Granbio, Inc. has devices listed in FDA 510(k) (7 devices).
What risk classes do Granbio, Inc.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Granbio, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Granbio, Inc. in the registry?
The most recently registered devices listed for Granbio, Inc. include EBNA ACIF ASSAY KIT, (EIA) FOR IGM ANTIBODY TO EBV VCA IN HUMAN SERUM, INDIRECT IMMUNOFLUORESCENT ANTIBODY ASSAY and EBV VCA IGM ANTIBODY ASSAY KIT.