Collaboration Live

System, Image Processing, Radiological

Philips Healthcare

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

Pre-market Notification Details

• Device ID: K200179
• 510k Number: K200179
• Device Name: Collaboration Live
• Classification: System, Image Processing, Radiological
• Applicant: Philips Healthcare 22100 Bothell Everett Highway Bothell, WA 98021 -8431
• Contact: Paul Elias
• Correspondent: Prithul Bom; REGULATORY TECHNOLOGY SERVICES, LLC 1000 Westgate Drive, Suite 510k Saint Paul, MN 55114
• Product Code: LLZ
• Subsequent Product Code: IYN
• Subsequent Product Code: IYO
• CFR Regulation Number: 892.2050 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: Yes
• Combination Product: No
• Date Received: 2020-01-24
• Decision Date: 2020-02-18