Kb & Assoc.
Country not established
- Devices
- 1
What Kb & Assoc. makes
Kb & Assoc. manufactures the Life Line, a medical device designed for patient monitoring or emergency response in clinical or home settings.
The Life Line is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Life Line Ref K830254
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kb & Assoc. have in the registry?
The registry currently lists 1 device for Kb & Assoc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kb & Assoc.'s devices?
Among its 1 most recently registered device, Kb & Assoc. has devices listed in FDA 510(k) (1 device).
What risk classes do Kb & Assoc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Kb & Assoc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kb & Assoc. in the registry?
The most recently registered devices listed for Kb & Assoc. include LIFE LINE.