Kal Life Systems
Country not established
- Devices
- 1
What Kal Life Systems makes
Kal Life Systems manufactures the LOGIKAL Lontophoresis Unit, a device designed for anesthesia inotophoresis, which delivers medication transdermally using iontophoresis technology.
The LOGIKAL Lontophoresis Unit is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kal Life Systems have in the registry?
The registry currently lists 1 device for Kal Life Systems. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kal Life Systems's devices?
Among its 1 most recently registered device, Kal Life Systems has devices listed in FDA 510(k) (1 device).
What risk classes do Kal Life Systems's devices fall under?
Among its 1 most recently registered device, the classes recorded for Kal Life Systems's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kal Life Systems in the registry?
The most recently registered devices listed for Kal Life Systems include LOGIKAL LONTOPHORESIS UNIT -ANESTHESIA INOTOPHORES.