Kcbiomedix, Inc.
Country not established
- Devices
- 1
What Kcbiomedix, Inc. makes
Kcbiomedix, Inc. manufactures the NTRAINER SYSTEM, a medical device designed for training and simulation in a clinical or educational setting, likely used to practice procedural techniques or patient care scenarios.
The NTRAINER SYSTEM is classified as a Class II device under FDA regulations and is listed via the 510(k) clearance pathway. The company is based in the United States.
Catalogue
Ntrainer System Ref K071866
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kcbiomedix, Inc. have in the registry?
The registry currently lists 1 device for Kcbiomedix, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kcbiomedix, Inc.'s devices?
Among its 1 most recently registered device, Kcbiomedix, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Kcbiomedix, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Kcbiomedix, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kcbiomedix, Inc. in the registry?
The most recently registered devices listed for Kcbiomedix, Inc. include NTRAINER SYSTEM.