Leon H. Lang Co.
AustriaFDA applicant, unverified
- Devices
- 1
What Leon H. Lang Co. makes
Leon H. Lang Co. manufactures SKINTACT AG electrodes, which are adhesive electrodes designed for use in electrotherapy and electrodiagnostic procedures, including electromyography (EMG) and nerve conduction studies.
These electrodes are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Skintact AG Electrodes Ref K862618
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Leon H. Lang Co. have in the registry?
The registry currently lists 1 device for Leon H. Lang Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Leon H. Lang Co.'s devices?
Among its 1 most recently registered device, Leon H. Lang Co. has devices listed in FDA 510(k) (1 device).
What risk classes do Leon H. Lang Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Leon H. Lang Co.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Leon H. Lang Co. in the registry?
The most recently registered devices listed for Leon H. Lang Co. include SKINTACT AG ELECTRODES.