MIMVIEWER

System, Image Processing, Radiological

MIMVISTA CORP.

The following data is part of a premarket notification filed by Mimvista Corp. with the FDA for Mimviewer.

Pre-market Notification Details

• Device ID: K062163
• 510k Number: K062163
• Device Name: MIMVIEWER
• Classification: System, Image Processing, Radiological
• Applicant: MIMVISTA CORP. 25200 CHAGRIN BLVD. SUITE 200 Cleveland, OH 44122
• Contact: Peter Simmelink
• Correspondent: Peter Simmelink; MIMVISTA CORP. 25200 CHAGRIN BLVD. SUITE 200 Cleveland, OH 44122
• Product Code: LLZ
• CFR Regulation Number: 892.2050 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2006-07-28
• Decision Date: 2006-09-22
• Summary: summary