Stihler Electronic, C/O Worldwide Regul. Services
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- Devices
- 1
What Stihler Electronic, C/O Worldwide Regul. Services makes
Stihler Electronic makes the STIHLER ASTOTHERM IFT 200 and IFT 220 devices, which are infrared therapy units used for delivering targeted heat treatment.
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
Stihler Astotherm Ift 200, Ift 220 Ref K882361
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Stihler Electronic, C/O Worldwide Regul. Services have in the registry?
The registry currently lists 1 device for Stihler Electronic, C/O Worldwide Regul. Services. Devices recorded under merged duplicate company entries are counted once.
Which registries list Stihler Electronic, C/O Worldwide Regul. Services's devices?
Among its 1 most recently registered device, Stihler Electronic, C/O Worldwide Regul. Services has devices listed in FDA 510(k) (1 device).
What risk classes do Stihler Electronic, C/O Worldwide Regul. Services's devices fall under?
Among its 1 most recently registered device, the classes recorded for Stihler Electronic, C/O Worldwide Regul. Services's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Stihler Electronic, C/O Worldwide Regul. Services in the registry?
The most recently registered devices listed for Stihler Electronic, C/O Worldwide Regul. Services include STIHLER ASTOTHERM IFT 200, IFT 220.