Clrs Technology Corporation
United StatesFDA applicant, unverified
- Devices
- 2
What Clrs Technology Corporation makes
Clrs Technology Corporation manufactures the CLARO, a medical device designed for diagnostic imaging and analysis, specifically targeting applications in radiology and interventional procedures. The device is intended to enhance visualization and guidance during procedures such as angiography and other vascular interventions.
The CLARO falls under FDA Class II regulation and has been submitted for 510(k) clearance in the United States. The company is headquartered in the US, where its devices are subject to compliance with the FDA’s regulatory requirements.
Catalogue
Frequently asked questions
How many devices does Clrs Technology Corporation have in the registry?
The registry currently lists 2 devices for Clrs Technology Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Clrs Technology Corporation's devices?
Among its 2 most recently registered devices, Clrs Technology Corporation has devices listed in FDA 510(k) (2 devices).
What risk classes do Clrs Technology Corporation's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Clrs Technology Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Clrs Technology Corporation in the registry?
The most recently registered devices listed for Clrs Technology Corporation include CLARO.