Ketronic, Inc.
Country not established
- Devices
- 10
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Tredband Type I, It, Ii & Iii - Treadmills Ref K850871
Regimes: 510(k) Registry: 510(k)Mfe Cardiac Stress System Ref K850868
Regimes: 510(k) Registry: 510(k)Ketronic Medax - N Ref K843288
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Ligtvoet L80.2 Lightfoot L80.2 Power Wheelchair Ref K850876
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Action-Wheels & Play Wheels Ref K850875
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Mfe Couch Ergometer Ref K850869
Regimes: 510(k) Registry: 510(k)Medifette Ergometer Ref K850870
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ketronic, Inc. have in the registry?
The registry currently lists 10 devices for Ketronic, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ketronic, Inc.'s devices?
Among its 10 most recently registered devices, Ketronic, Inc. has devices listed in FDA 510(k) (10 devices).
What risk classes do Ketronic, Inc.'s devices fall under?
Among its 10 most recently registered devices, the classes recorded for Ketronic, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ketronic, Inc. in the registry?
The most recently registered devices listed for Ketronic, Inc. include TREDBAND TYPE I, IT, II & III - TREADMILLS, MFE CARDIAC STRESS SYSTEM, KETRONIC MEDAX - N and MONOLIFT MPE2, PLATFORM, CHAIR, FULLY FUTO PLATFOR.