Halkey-Roberts Corporation
Also registered as Halkey-Roberts Corp.
United Statesfrom the FDA registration address FDA establishment FEI 1000324175
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Robertsite Stopcock Ref K061143
Regimes: 510(k) Registry: 510(k)Robertsite Vial Adapter, Model 245700021 Ref K040634
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 1000324175
- Address
- 2700 Halkey-Roberts Place North, Saint Petersburg, FL, 33716
Frequently asked questions
How many devices does Halkey-Roberts Corporation have in the registry?
The registry currently lists 2 devices for Halkey-Roberts Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Halkey-Roberts Corporation's devices?
Among its 2 most recently registered devices, Halkey-Roberts Corporation has devices listed in FDA 510(k) (2 devices).
What risk classes do Halkey-Roberts Corporation's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Halkey-Roberts Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Halkey-Roberts Corporation in the registry?
The most recently registered devices listed for Halkey-Roberts Corporation include ROBERTSITE STOPCOCK and ROBERTSITE VIAL ADAPTER, MODEL 245700021.