SOFTNETA is proud to announce that MedDream WEB DICOM Viewer is FDA cleared for diagnostic use.

FDA 510(k) clearance for MedDream as a class II medical device.

Indications for Use:
MedDream is a software medical imaging system used to receive DICOM images, scheduling information and textual reports, organize and store them in an internal format, and to make that information available across a network via web and customized user interfaces. Software is intended for use as a diagnostic, review, and analysis tool by trained professionals such as radiologists, physicians, clinicians.

Contraindications: The MedDream is not intended for the acquisition of mammographic image data and is meant to be used by qualified medical personnel only who are qualified to create and diagnose medical image data.