The Austin-Lenick Co.
Country not established
- Devices
- 1
What The Austin-Lenick Co. makes
The Austin-Lenick Co. manufactures the Stimutron Model 100, which is a medical device.
This product is classified as a Class II device and is listed in the FDA 510(k) registry, with the company based in the United States.
Catalogue
Stimutron Model 100 Ref K865054
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does The Austin-Lenick Co. have in the registry?
The registry currently lists 1 device for The Austin-Lenick Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list The Austin-Lenick Co.'s devices?
Among its 1 most recently registered device, The Austin-Lenick Co. has devices listed in FDA 510(k) (1 device).
What risk classes do The Austin-Lenick Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for The Austin-Lenick Co.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from The Austin-Lenick Co. in the registry?
The most recently registered devices listed for The Austin-Lenick Co. include STIMUTRON MODEL 100.