Skedco, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Skedco, Inc. makes
Skedco, Inc. manufactures the SKED Stretcher, a lightweight patient transport device designed for rapid movement in emergency and field settings, and the SKED Flotation System, a buoyancy aid for water-based rescues and evacuations.
The company’s products are classified as Class I medical devices under FDA regulations and are supported by 510(k) clearances. Skedco, Inc. is based in the United States.
Catalogue
Sked Stretcher Ref K896177
Regimes: 510(k) Registry: 510(k)Sked Flotation System Ref K896179
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Skedco, Inc. have in the registry?
The registry currently lists 2 devices for Skedco, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Skedco, Inc.'s devices?
Among its 2 most recently registered devices, Skedco, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Skedco, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Skedco, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Skedco, Inc. in the registry?
The most recently registered devices listed for Skedco, Inc. include SKED STRETCHER and SKED FLOTATION SYSTEM.