James K. Brannon
Country not established
- Devices
- 2
What James K. Brannon makes
James K. Brannon manufactures pre-filled syringe devices, including pediatric and standard-sized portsyringes designed for medication administration.
These products are classified as Class II medical devices and are listed in the FDA’s 510(k) registry. The manufacturer operates from the United States.
Catalogue
Brannon Pedi Portsyringe Ref K960047
Regimes: 510(k) Registry: 510(k)Brannon Portsyringe Ref K960049
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does James K. Brannon have in the registry?
The registry currently lists 2 devices for James K. Brannon. Devices recorded under merged duplicate company entries are counted once.
Which registries list James K. Brannon's devices?
Among its 2 most recently registered devices, James K. Brannon has devices listed in FDA 510(k) (2 devices).
What risk classes do James K. Brannon's devices fall under?
Among its 2 most recently registered devices, the classes recorded for James K. Brannon's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from James K. Brannon in the registry?
The most recently registered devices listed for James K. Brannon include BRANNON PEDI PORTSYRINGE and BRANNON PORTSYRINGE.