Sweden Diagnostics (US), Inc.
Country not established
- Devices
- 1
What Sweden Diagnostics (US), Inc. makes
Sweden Diagnostics (Us), Inc. manufactures the ELIA CCP and the ELIA CCP Control, which are diagnostic products used for laboratory testing.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) database. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sweden Diagnostics (Us), Inc. have in the registry?
The registry currently lists 1 device for Sweden Diagnostics (Us), Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sweden Diagnostics (Us), Inc.'s devices?
Among its 1 most recently registered device, Sweden Diagnostics (Us), Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Sweden Diagnostics (Us), Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Sweden Diagnostics (Us), Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sweden Diagnostics (Us), Inc. in the registry?
The most recently registered devices listed for Sweden Diagnostics (Us), Inc. include ELIA CCP, MODEL 14-5515-01; ELIA CCP CONTROL, MODEL 83-1009-01.