Elixir Corporation
United Statesfrom the FDA registration address FDA FEI 3008513006
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Abc Syringe Infusion Pump, Model 4100 Ref K072603
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3008513006
- Address
- 305 Shawnee North Dr Ste 250, Suwanee, GA, 30024
Frequently asked questions
How many devices does Elixir Corporation have in the registry?
The registry currently lists 1 device for Elixir Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Elixir Corporation's devices?
Among its 1 most recently registered device, Elixir Corporation has devices listed in FDA 510(k) (1 device).
What risk classes do Elixir Corporation's devices fall under?
Among its 1 most recently registered device, the classes recorded for Elixir Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Elixir Corporation in the registry?
The most recently registered devices listed for Elixir Corporation include ABC SYRINGE INFUSION PUMP, MODEL 4100.