# K212777: Collaboration Live

- Pathway: 510(k) (Special)
- Applicant: Philips Ultrasound, Inc.
- Decided: Sep 24, 2021 after 23 days
- Product code: LLZ (System, Image Processing, Radiological)
- Device class: 2
- Regulation: 21 CFR 892.2050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 8 generations back to K971684 (1997). 31 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 33 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K201665: Collaboration Live, Philips Ultrasound, Inc. (2020) Summary page 4.

## Most influential descendants
- K241302: SonoSync (2024), 0 descendants of its own

## Indications for use
Collaboration Live is indicated for remote console access of the Philips ultrasound system for diagnostic image viewing and review, consultation, guidance, support, and education in real time. Access must be granted by the healthcare professionals operating the ultrasound system. Compliance with the technical and operator requirements specified in the User Manual is required. It is the responsibility of the healthcare professionals at the remote client to ensure image quality, display contrast, and ambient light conditions are consistent with the generally accepted standards of the clinical application.

Source page: https://510kreport.com/device/K212777
Methodology: https://510kreport.com/methodology