Kika Medical, Inc.
Country not established
- Devices
- 1
What Kika Medical, Inc. makes
Kika Medical, Inc. develops the KIKA IMAGING LAB VIEWER, a software application designed for medical imaging review and analysis in clinical settings.
The company’s portfolio is regulated under FDA’s Class II device classification and is listed in the FDA’s 510(k) clearance registry. The manufacturer is based in the United States.
Catalogue
Kika Imaging Lab Viewer, Model 2.0.1.0 Ref K051127
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kika Medical, Inc. have in the registry?
The registry currently lists 1 device for Kika Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kika Medical, Inc.'s devices?
Among its 1 most recently registered device, Kika Medical, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Kika Medical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Kika Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kika Medical, Inc. in the registry?
The most recently registered devices listed for Kika Medical, Inc. include KIKA IMAGING LAB VIEWER, MODEL 2.0.1.0.