Westport Mobility Products, Inc.
CanadaFDA applicant, unverified
- Devices
- 1
What Westport Mobility Products, Inc. makes
Westport Mobility Products, Inc. manufactures The Adventurer, a mobility aid designed for outdoor use, intended to assist individuals with limited mobility in navigating trails and natural terrains.
The Adventurer is classified as Class I under FDA regulations and is listed via 510(k) clearance. The company is based in the United States.
Catalogue
The Adventurer Ref K881410
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Westport Mobility Products, Inc. have in the registry?
The registry currently lists 1 device for Westport Mobility Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Westport Mobility Products, Inc.'s devices?
Among its 1 most recently registered device, Westport Mobility Products, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Westport Mobility Products, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Westport Mobility Products, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Westport Mobility Products, Inc. in the registry?
The most recently registered devices listed for Westport Mobility Products, Inc. include THE ADVENTURER.