K231482 is an FDA 510(k) clearance for the uCT ATLAS Astound with uWS-CT-Dual Energy Analysis, uCT ATLAS with uWS-CT-Dual Energy Analysis. This device is classified as a System, X-ray, Tomography, Computed (Class II - Special Controls, product code JAK).
Submitted by Shanghai United Imaging Healthcare Co., Ltd. (Shanghai, CN). The FDA issued a Cleared decision on November 29, 2023, 190 days after receiving the submission on May 23, 2023.
This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.1750.