Kim Institute For Rehabilitation Medicine, P.C.
Country not established
- Devices
- 1
What Kim Institute For Rehabilitation Medicine, P.C. makes
The Kim Institute for Rehabilitation Medicine, P.C. manufactures the KIMSTIM Auricular Electrode, a device used for transcutaneous electrical nerve stimulation (TENS) applied to the auricular (ear) region for therapeutic purposes.
This product is classified as a Class II medical device in the U.S. and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Kimstim Auricular Electrode Ref K011691
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kim Institute For Rehabilitation Medicine, P.C. have in the registry?
The registry currently lists 1 device for Kim Institute For Rehabilitation Medicine, P.C.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kim Institute For Rehabilitation Medicine, P.C.'s devices?
Among its 1 most recently registered device, Kim Institute For Rehabilitation Medicine, P.C. has devices listed in FDA 510(k) (1 device).
What risk classes do Kim Institute For Rehabilitation Medicine, P.C.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Kim Institute For Rehabilitation Medicine, P.C.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kim Institute For Rehabilitation Medicine, P.C. in the registry?
The most recently registered devices listed for Kim Institute For Rehabilitation Medicine, P.C. include KIMSTIM AURICULAR ELECTRODE.