Hausted, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Hausted, Inc. makes
Hausted, Inc. makes surgical stretchers and patient positioning devices, including the Model 578 Mobile Surgical Stretcher, Model 792 Converge, and Model 793 Vision 2000.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Model 792 Converge, Model 793 Vision 2000 Ref K945431
Regimes: 510(k) Registry: 510(k)Model 578 Mobile Surgical Stretcher Ref K943969
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hausted, Inc. have in the registry?
The registry currently lists 2 devices for Hausted, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hausted, Inc.'s devices?
Among its 2 most recently registered devices, Hausted, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Hausted, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Hausted, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hausted, Inc. in the registry?
The most recently registered devices listed for Hausted, Inc. include MODEL 792 CONVERGE, MODEL 793 VISION 2000 and MODEL 578 MOBILE SURGICAL STRETCHER.