Liberator Wheelchairs, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Liberator Wheelchairs, Inc. makes
Liberator Wheelchairs, Inc. manufactures manual wheelchairs designed for mobility assistance, including models like *The Liberator Wheelchair* and *The Liberator*. These devices are intended for indoor and outdoor use, providing adjustable seating and frame configurations to accommodate different user needs and environments.
The company’s products are classified as Class II medical devices under U.S. regulations and are listed in the FDA’s 510(k) registry. The portfolio is regulated under the U.S. Food and Drug Administration’s premarket notification process, ensuring compliance with safety and performance standards for mobility aids.
Catalogue
The Liberator Wheelchair Ref K010859
Regimes: 510(k) Registry: 510(k)The Liberator Ref K984391
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Liberator Wheelchairs, Inc. have in the registry?
The registry currently lists 2 devices for Liberator Wheelchairs, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Liberator Wheelchairs, Inc.'s devices?
Among its 2 most recently registered devices, Liberator Wheelchairs, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Liberator Wheelchairs, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Liberator Wheelchairs, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Liberator Wheelchairs, Inc. in the registry?
The most recently registered devices listed for Liberator Wheelchairs, Inc. include THE LIBERATOR WHEELCHAIR and THE LIBERATOR.