Panion & BF Biotech, Inc.
TaiwanFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Vstrip H. pylori Antigen Rapid Test Ref K183573
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Panion & BF Biotech, Inc. have in the registry?
The registry currently lists 1 device for Panion & BF Biotech, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Panion & BF Biotech, Inc.'s devices?
Among its 1 most recently registered device, Panion & BF Biotech, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Panion & BF Biotech, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Panion & BF Biotech, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Panion & BF Biotech, Inc. in the registry?
The most recently registered devices listed for Panion & BF Biotech, Inc. include Vstrip H. pylori Antigen Rapid Test.