Cumes-Honikman Partnership
Country not established
- Devices
- 1
What Cumes-Honikman Partnership makes
The Cumes-Honikman Partnership manufactures CUMEVAC, a Class I medical device designed for vaccination purposes, likely involving the administration or formulation of vaccines.
CUMEVAC is regulated under the FDA’s 510(k) pathway as a Class I device and is listed in the U.S. regulatory registry. The company is based in the United States.
Catalogue
Cumevac Ref K874410
510(k) 510(k)
Frequently asked questions
How many devices does Cumes-Honikman Partnership have in the registry?
The registry currently lists 1 device for Cumes-Honikman Partnership. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cumes-Honikman Partnership's devices?
Among its 1 most recently registered device, Cumes-Honikman Partnership has devices listed in FDA 510(k) (1 device).
What risk classes do Cumes-Honikman Partnership's devices fall under?
Among its 1 most recently registered device, the classes recorded for Cumes-Honikman Partnership's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Cumes-Honikman Partnership in the registry?
The most recently registered devices listed for Cumes-Honikman Partnership include CUMEVAC.