Stumark Corp.
Country not established
- Devices
- 1
What Stumark Corp. makes
Stumark Corp. manufactures the Stumark Infusor, a Class II medical device designed for controlled administration of fluids or medications into the body.
The Stumark Infusor is regulated under the FDA’s 510(k) pathway as a Class II device and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Stumark Infusor Ref K810252
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Stumark Corp. have in the registry?
The registry currently lists 1 device for Stumark Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Stumark Corp.'s devices?
Among its 1 most recently registered device, Stumark Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Stumark Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Stumark Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Stumark Corp. in the registry?
The most recently registered devices listed for Stumark Corp. include STUMARK INFUSOR.