Collaboration Live

System, Image Processing, Radiological

Philips Ultrasound, Inc.

The following data is part of a premarket notification filed by Philips Ultrasound, Inc. with the FDA for Collaboration Live.

Pre-market Notification Details

• Device ID: K212777
• 510k Number: K212777
• Device Name: Collaboration Live
• Classification: System, Image Processing, Radiological
• Applicant: Philips Ultrasound, Inc. 22100 Bothell Everett Highway Bothell, WA 98201 -8431
• Contact: Courtney Nix
• Correspondent: Tamara Daniels; Philips Ultrasound, Inc 22100 Bothell Everett Highway Bothell, WA 98201 -8432
• Product Code: LLZ
• Subsequent Product Code: IYN
• Subsequent Product Code: IYO
• CFR Regulation Number: 892.2050 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Special
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2021-09-01
• Decision Date: 2021-09-24