Clearcanvas, Inc.
CanadaFDA applicant, unverified
- Devices
- 1
What Clearcanvas, Inc. makes
Clearcanvas, Inc. develops and provides the CLEARCANVAS RIS (Radiology Information System) and PACS (Picture Archiving and Communication System) software solutions, which integrate radiology workflows and digital imaging storage for healthcare facilities.
These products are classified as Class II medical devices under FDA regulations and are authorised via the 510(k) clearance process. The company is based in the United States.
Catalogue
Clearcanvas Ris / Pacs Ref K110332
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Clearcanvas, Inc. have in the registry?
The registry currently lists 1 device for Clearcanvas, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Clearcanvas, Inc.'s devices?
Among its 1 most recently registered device, Clearcanvas, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Clearcanvas, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Clearcanvas, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Clearcanvas, Inc. in the registry?
The most recently registered devices listed for Clearcanvas, Inc. include CLEARCANVAS RIS / PACS.