Atad Developments, Ltd.
IsraelFDA 510(k) applicant, unverified
- Devices
- 1
What Atad Developments, Ltd. makes
Atad Developments, Ltd. manufactures the ATAD ARD Catheter, a medical device designed for specific vascular or interventional procedures.
The ATAD ARD Catheter is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Atad Ard Catheter Ref K040625
510(k) 510(k)
Frequently asked questions
How many devices does Atad Developments, Ltd. have in the registry?
The registry currently lists 1 device for Atad Developments, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Atad Developments, Ltd.'s devices?
Among its 1 most recently registered device, Atad Developments, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Atad Developments, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Atad Developments, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Atad Developments, Ltd. in the registry?
The most recently registered devices listed for Atad Developments, Ltd. include ATAD ARD CATHETER.