IMAGEQUEST

System, Digital Image Communications, Radiological

VISUAL MED, INC.

The following data is part of a premarket notification filed by Visual Med, Inc. with the FDA for Imagequest.

Pre-market Notification Details

• Device ID: K974707
• 510k Number: K974707
• Device Name: IMAGEQUEST
• Classification: System, Digital Image Communications, Radiological
• Applicant: VISUAL MED, INC. 3695 CENTRE CIRCLE DR. Ft. Mill, SC 29715
• Product Code: LMD
• CFR Regulation Number: 892.2020 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1997-12-16
• Decision Date: 1998-07-31