Bioject, Inc.
United StatesFDA applicant, unverified
- Devices
- 9
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Zetajet Ref K090003
Regimes: 510(k) Registry: 510(k)Serojet Ref K003908
Regimes: 510(k) Registry: 510(k)Clicker Ref K994384
Regimes: 510(k) Registry: 510(k)Biojector 2000 Model 1B02000 Ref K960373
Regimes: 510(k) Registry: 510(k)Bioject Jet Injection System Ref K920631
Regimes: 510(k) Registry: 510(k)Cool.click Ref K050734
Regimes: 510(k) Registry: 510(k)Bioject Needle-Free Vial Adapter (13mm) Ref K963012
Regimes: 510(k) Registry: 510(k)Biojector Syringe System Ref K861687
Regimes: 510(k) Registry: 510(k)Reconstitution Kit & Vial Connector Ref K010623
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bioject, Inc. have in the registry?
The registry currently lists 9 devices for Bioject, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bioject, Inc.'s devices?
Among its 9 most recently registered devices, Bioject, Inc. has devices listed in FDA 510(k) (9 devices).
What risk classes do Bioject, Inc.'s devices fall under?
Among its 9 most recently registered devices, the classes recorded for Bioject, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bioject, Inc. in the registry?
The most recently registered devices listed for Bioject, Inc. include ZETAJET, SEROJET, CLICKER and BIOJECTOR 2000 MODEL 1B02000.