Saab-Scania of America, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Saab-Scania of America, Inc. makes
Saab-Scania of America, Inc. manufactures mobility devices including the Permobil Exterior and Permobil Superior, which are power wheelchairs designed for outdoor and indoor use respectively.
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
Permobil Exterior Ref K790858
Regimes: 510(k) Registry: 510(k)Permobil Superior Ref K790859
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Saab-Scania of America, Inc. have in the registry?
The registry currently lists 2 devices for Saab-Scania of America, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Saab-Scania of America, Inc.'s devices?
Among its 2 most recently registered devices, Saab-Scania of America, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Saab-Scania of America, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Saab-Scania of America, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Saab-Scania of America, Inc. in the registry?
The most recently registered devices listed for Saab-Scania of America, Inc. include PERMOBIL EXTERIOR and PERMOBIL SUPERIOR.