Pro Walker, Inc.
TaiwanFDA applicant, unverified
- Devices
- 2
What Pro Walker, Inc. makes
Pro Walker, Inc. manufactures mobility aids, including the PRO WALKER PL-200 Power Wheelchair—an electrically powered wheelchair for users requiring motorised assistance—and the PRO WALKER ML-300 Foldable Wheelchair, a manual folding wheelchair designed for transport and storage.
The company’s devices are regulated under FDA Class I (general controls) and Class II (special controls) requirements, with some models requiring 510(k) clearance for market authorisation. These products are listed in the FDA’s 510(k) database, and the company is based in the United States.
Catalogue
Pro Walker Pl-200 Power Wheelchair Ref K041336
Regimes: 510(k) Registry: 510(k)Pro Walker Ml-300 Foldable Wheelchair Ref K041337
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pro Walker, Inc. have in the registry?
The registry currently lists 2 devices for Pro Walker, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pro Walker, Inc.'s devices?
Among its 2 most recently registered devices, Pro Walker, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Pro Walker, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Pro Walker, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pro Walker, Inc. in the registry?
The most recently registered devices listed for Pro Walker, Inc. include PRO WALKER PL-200 POWER WHEELCHAIR and PRO WALKER ML-300 FOLDABLE WHEELCHAIR.