Cushman Mfg., Inc.
Country not established
- Devices
- 1
What Cushman Mfg., Inc. makes
Cushman Manufacturing, Inc. produces the ULTRA 6.0, a Class II medical device designed for patient positioning and support in clinical settings, such as operating rooms and recovery areas.
The ULTRA 6.0 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
Cushman Manufacturing, Inc. Ultra 6.0. Ref K960802
510(k) 510(k)
Frequently asked questions
How many devices does Cushman Mfg., Inc. have in the registry?
The registry currently lists 1 device for Cushman Mfg., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cushman Mfg., Inc.'s devices?
Among its 1 most recently registered device, Cushman Mfg., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Cushman Mfg., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Cushman Mfg., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cushman Mfg., Inc. in the registry?
The most recently registered devices listed for Cushman Mfg., Inc. include CUSHMAN MANUFACTURING, INC. ULTRA 6.0..