Rehab Technology, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Rehab Technology, Inc. makes
Rehab Technology, Inc. manufactures electronic control units for adaptive television systems, including the ECU 1218, as well as specialized television control options like the TELEVISION CONTROL OPTION 1219 and TELEVISION CONTROL OPTION 1220. They also produce the EXCELSIOR, a device designed for accessibility in television viewing, likely for individuals with mobility or dexterity limitations.
The company’s products fall under FDA Class II medical devices and are subject to 510(k) clearance requirements in the United States. These devices are listed in the FDA’s regulatory database under the 510(k) pathway, ensuring compliance with U.S. medical device regulations.
Catalogue
Ecu 1218 Ref K840808
Regimes: 510(k) Registry: 510(k)Television Control Option 1219 Ref K850313
Regimes: 510(k) Registry: 510(k)The Excelsior Ref K921084
Regimes: 510(k) Registry: 510(k)Television Control Option 1220 Ref K850314
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rehab Technology, Inc. have in the registry?
The registry currently lists 4 devices for Rehab Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rehab Technology, Inc.'s devices?
Among its 4 most recently registered devices, Rehab Technology, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Rehab Technology, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Rehab Technology, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Rehab Technology, Inc. in the registry?
The most recently registered devices listed for Rehab Technology, Inc. include ECU 1218, TELEVISION CONTROL OPTION 1219, THE EXCELSIOR and TELEVISION CONTROL OPTION 1220.