Digital x-ray firm Kub Technologies (Kubtec) has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its DigiView 250 digital radiography (DR) detector, which features complementary metal-oxide-semiconductor (CMOS) technology designed for low-dose and high-resolution imaging.
DigiView 250 is intended for neonatal, pediatric, and extremity imaging, according to Kubtec. The detector weighs less than 7 lb and is configured in a custom-molded plastic housing with an integrated handle for enhanced positioning. It also offers DICOM 3.0-compliant image enhancement tools, onscreen measurement capabilities, and the ability to annotate and send images to a PACS network.
