ImmersiveTouch

System, Image Processing, Radiological

ImmersiveTouch, Inc.

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

Pre-market Notification Details

• Device ID: K210726
• 510k Number: K210726
• Device Name: ImmersiveTouch
• Classification: System, Image Processing, Radiological
• Applicant: ImmersiveTouch, Inc. 910 W Van Buren St, Suite 715 Chicago, IL 60607
• Contact: P. Pat Banerjee
• Correspondent: P. Pat Banerjee; ImmersiveTouch, Inc. 910 W Van Buren St, Suite 715 Chicago, IL 60607
• Product Code: LLZ
• CFR Regulation Number: 892.2050 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2021-03-11
• Decision Date: 2021-09-29

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
B940IMMERSIVEVIEW50	K210726	000