Heliarc Specialists, Inc.
Country not established
- Devices
- 1
What Heliarc Specialists, Inc. makes
Heliarc Specialists, Inc. manufactures the Wheel Lemaster, a device designed for securing and stabilizing medical wheelchairs to prevent movement during transport or repositioning.
The Wheel Lemaster is classified as a Class I medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Wheel Lemaster Ref K954370
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Heliarc Specialists, Inc. have in the registry?
The registry currently lists 1 device for Heliarc Specialists, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Heliarc Specialists, Inc.'s devices?
Among its 1 most recently registered device, Heliarc Specialists, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Heliarc Specialists, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Heliarc Specialists, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Heliarc Specialists, Inc. in the registry?
The most recently registered devices listed for Heliarc Specialists, Inc. include WHEEL LEMASTER.