Aicheck Biotech, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Aicheck Biotech, Inc. have in the registry?
The registry currently lists 2 devices for Aicheck Biotech, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Aicheck Biotech, Inc.'s devices?
Among its 2 most recently registered devices, Aicheck Biotech, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Aicheck Biotech, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Aicheck Biotech, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Aicheck Biotech, Inc. in the registry?
The most recently registered devices listed for Aicheck Biotech, Inc. include PocguideTM Multi-Drug Test Cup OTC, PocguideTM Multi-Drug Test Cup and Pocguide Multi-Drug Test Panel, Pocguide Multi-Drug Test Panel OTC.