K973131 is an FDA 510(k) clearance for the SIENET MAGICWEB (WEB SERVER), SIENET MAGICLINK I (ISI-GATEWAY). This device is classified as a System, Digital Image Communications, Radiological (Class I - General Controls, product code LMD).
Submitted by Siemens Medical Solutions USA, Inc. (Iselin, US). The FDA issued a Cleared decision on November 12, 1997, 83 days after receiving the submission on August 21, 1997.
This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.2020. A Medical Image Communications Device Provides Electronic Transfer Of Medical Image Data Between Medical Devices. It May Include A Physical Communications Medium, Modems, Interfaces, And A Communications Protocol. It May Provide Simple Image Review Software Functionality For Medical Image Processing And Manipulation, Such As Grayscale Window And Level, Zoom And Pan, User Delineated Geometric Measurements, Compression, Or User Added Image Annotations. The Device Does Not Perform Advanced Image Processing Or Complex Quantitative Functions..