Adp, Ltd.
IsraelFDA applicant, unverified
- Devices
- 1
What Adp, Ltd. makes
Adp, Ltd. makes the ADVIEWER 2000, a medical device classified as Class I.
The ADVIEWER 2000 is listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Adviewer 2000 Ref K952188
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Adp, Ltd. have in the registry?
The registry currently lists 1 device for Adp, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Adp, Ltd.'s devices?
Among its 1 most recently registered device, Adp, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Adp, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Adp, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Adp, Ltd. in the registry?
The most recently registered devices listed for Adp, Ltd. include ADVIEWER 2000.