Ultralink, LLC
United StatesFDA applicant, unverified
- Devices
- 2
What Ultralink, LLC makes
Ultralink, LLC manufactures VHF ultrasonic arc-scan systems and the Artemis device, which are designed for medical imaging and diagnostic purposes.
These products fall under FDA Class II regulation and are listed via the 510(k) clearance pathway. The company is based in the United States.
Catalogue
Vhf Ultrasonic Arc-Scan System Ref K003890
Regimes: 510(k) Registry: 510(k)Artemis Ref K021333
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ultralink, LLC have in the registry?
The registry currently lists 2 devices for Ultralink, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ultralink, LLC's devices?
Among its 2 most recently registered devices, Ultralink, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do Ultralink, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Ultralink, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ultralink, LLC in the registry?
The most recently registered devices listed for Ultralink, LLC include VHF ULTRASONIC ARC-SCAN SYSTEM and ARTEMIS.