![FDA, FTC and DOJ Enforcement of Medical Device Regulations FDA, FTC and DOJ Enforcement of Medical Device Regulations](https://www.fdanews.com/ext/resources/Book-Covers-2/BFFDEMDR-COVER.png?height=200&t=1685733565&width=200)
Home » Carestream’s Dual-Energy Imaging Technology Cleared
Carestream’s Dual-Energy Imaging Technology Cleared
![ClearanceStamp_Blue.gif](https://www.fdanews.com/ext/resources/test/Device_Images6/ClearanceStamp_Blue.gif?t=1576043968&width=430)
Carestream received 510(k) clearance from the FDA for its Dual-Energy imaging technology and its Focus 35C Detector with image suite software.
The dual-energy system uses two filter materials that are automatically switched between the high- and low-energy exposures to produce a soft-tissue-only image with the bone structures removed, as well as a corresponding bone-only image.
The Focus 35C Detector with image suite software offers smaller facilities and specialty practices a way to use digital medical imaging. The software provides an image in a Picture Archiving and Communication System (PACS) format.
Upcoming Events
-
11Jul
-
18Jul
-
21Oct