Cdp, Ltd.
IsraelFDA applicant, unverified
- Devices
- 1
What Cdp, Ltd. makes
Cdp, Ltd. manufactures the CDP 5000, a Media and Distribution Center designed for use with the DiagNet system. This device is intended for managing and distributing diagnostic imaging media within healthcare settings.
The CDP 5000 is classified as a Class II medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Cdp 5000, Media And Distribution Center, Diagnet Ref K072960
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cdp, Ltd. have in the registry?
The registry currently lists 1 device for Cdp, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cdp, Ltd.'s devices?
Among its 1 most recently registered device, Cdp, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Cdp, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Cdp, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cdp, Ltd. in the registry?
The most recently registered devices listed for Cdp, Ltd. include CDP 5000, MEDIA AND DISTRIBUTION CENTER, DIAGNET.