Techlab Inc., Corporate Research Center
United StatesFDA applicant, unverified
- Devices
- 5
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Asca-Chek Ref K071711
Regimes: 510(k) Registry: 510(k)Shiga Toxin Chek Ref K121411
Regimes: 510(k) Registry: 510(k)Leuko Ez Vue Ref K071712
Regimes: 510(k) Registry: 510(k)Shiga Toxin Quik Chek Ref K121364
Regimes: 510(k) Registry: 510(k)Giardia/ Cryptosporidium Quik Chek Ref K103673
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Techlab Inc., Corporate Research Center have in the registry?
The registry currently lists 5 devices for Techlab Inc., Corporate Research Center. Devices recorded under merged duplicate company entries are counted once.
Which registries list Techlab Inc., Corporate Research Center's devices?
Among its 5 most recently registered devices, Techlab Inc., Corporate Research Center has devices listed in FDA 510(k) (5 devices).
What risk classes do Techlab Inc., Corporate Research Center's devices fall under?
Among its 5 most recently registered devices, the classes recorded for Techlab Inc., Corporate Research Center's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Techlab Inc., Corporate Research Center in the registry?
The most recently registered devices listed for Techlab Inc., Corporate Research Center include ASCA-CHEK, SHIGA TOXIN CHEK, LEUKO EZ VUE and SHIGA TOXIN QUIK CHEK.