Northwind Technologies, Corp.
Country not established
- Devices
- 1
What Northwind Technologies, Corp. makes
Northwind Technologies, Corp. manufactures mobile intravenous (IV) systems, specifically the MOBILE I.V. SYSTEMS 10, 20, and 60 models.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Mobile I.V. Systems 10, 20, 60 Ref K080695
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Northwind Technologies, Corp. have in the registry?
The registry currently lists 1 device for Northwind Technologies, Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Northwind Technologies, Corp.'s devices?
Among its 1 most recently registered device, Northwind Technologies, Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Northwind Technologies, Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Northwind Technologies, Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Northwind Technologies, Corp. in the registry?
The most recently registered devices listed for Northwind Technologies, Corp. include MOBILE I.V. SYSTEMS 10, 20, 60.