The University of Chicago
Country not established
- Devices
- 2
What The University of Chicago makes
The University of Chicago manufactures pre-filled syringes designed for heparin administration and syringes specifically for blood sampling. These devices are intended for single-use medical procedures requiring precise dosing or fluid extraction.
The portfolio includes Class II devices, which are regulated under the FDA’s 510(k) clearance process. These products are listed in the FDA’s 510(k) registry and are intended for use within the United States.
Catalogue
Preheparinzed Syringe Ref K803302
Regimes: 510(k) Registry: 510(k)Syringe For Blood Sampling Ref K803182
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does The University of Chicago have in the registry?
The registry currently lists 2 devices for The University of Chicago. Devices recorded under merged duplicate company entries are counted once.
Which registries list The University of Chicago's devices?
Among its 2 most recently registered devices, The University of Chicago has devices listed in FDA 510(k) (2 devices).
What risk classes do The University of Chicago's devices fall under?
Among its 2 most recently registered devices, the classes recorded for The University of Chicago's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from The University of Chicago in the registry?
The most recently registered devices listed for The University of Chicago include PREHEPARINZED SYRINGE and SYRINGE FOR BLOOD SAMPLING.