Living Data Technologies Corporation
United StatesFDA applicant, unverified
- Devices
- 2
What Living Data Technologies Corporation makes
Living Data Technologies Corporation manufactures external counter-pulsation systems, including the AngioNEW-V mobile device and the AngioNEW-IV infusion-based model. These devices are designed to augment peripheral blood flow through timed compression and decompression of the lower extremities, intended for patients with peripheral artery disease or other circulatory conditions.
The company’s products are classified as Class II devices under FDA regulations and are listed via 510(k) clearance. The portfolio is authorised for commercial distribution in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Angionew-Iv Ref K023701
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Living Data Technologies Corporation have in the registry?
The registry currently lists 2 devices for Living Data Technologies Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Living Data Technologies Corporation's devices?
Among its 2 most recently registered devices, Living Data Technologies Corporation has devices listed in FDA 510(k) (2 devices).
What risk classes do Living Data Technologies Corporation's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Living Data Technologies Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Living Data Technologies Corporation in the registry?
The most recently registered devices listed for Living Data Technologies Corporation include MOBILE EXTERNAL COUNTER PULSATION SYSTEM ANGIONEW-V and ANGIONEW-IV.