Thyssenkrupp Accessibility B.V.
NetherlandsFDA applicant, unverified
- Devices
- 2
What Thyssenkrupp Accessibility B.V. makes
Thyssenkrupp Accessibility B.V. manufactures electric and manual patient lifts, including the FLOW2 and SWING models for hospital and clinical use, as well as the LEVANT and HOMEGLIDE series designed for home healthcare and mobility assistance.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
FLOW2, Swing Ref K121561
Regimes: 510(k) Registry: 510(k)Levant, Homeglide Ref K121560
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Thyssenkrupp Accessibility B.V. have in the registry?
The registry currently lists 2 devices for Thyssenkrupp Accessibility B.V.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Thyssenkrupp Accessibility B.V.'s devices?
Among its 2 most recently registered devices, Thyssenkrupp Accessibility B.V. has devices listed in FDA 510(k) (2 devices).
What risk classes do Thyssenkrupp Accessibility B.V.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Thyssenkrupp Accessibility B.V.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Thyssenkrupp Accessibility B.V. in the registry?
The most recently registered devices listed for Thyssenkrupp Accessibility B.V. include FLOW2, SWING and LEVANT, HOMEGLIDE.