Identifiers
- 510(k) Number
- K242329 FDA 510(k)
- FDA Product Code
- LLZ FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 892.2050 FDA 510(k)
- Regulation Number
- 892.2050 FDA 510(k)
- Advisory Committee
- Radiology FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
CT Collaboration Live is a telemedicine tool designed to facilitate remote consultation and training for CT systems. It enables users to connect with peers through chat, voice calls, video calls, screen sharing, and remote system access.
This device is supplied by Philips Healthcare (Suzhou) Co., Ltd. and has received FDA 510(k) clearance. It is intended to support real-time communication and remote clinical collaboration between care team members.
Frequently asked questions
What is the primary function of CT Collaboration Live?
This device is a telemedicine tool intended to support real-time communication and remote clinical collaboration between care team members. It facilitates remote consultation and training for CT systems through features such as chat, voice and video calls, screen sharing, and remote system access.
What is the regulatory status of this device?
CT Collaboration Live has received FDA 510(k) clearance under the K-number K242329. This indicates that the device has been determined to be substantially equivalent to a predicate device for its intended use in remote clinical collaboration.
Who is the manufacturer of this telemedicine tool?
The device is manufactured by Philips Healthcare (Suzhou) Co., Ltd., located in the Suzhou Industrial Park, Jiangsu, China. They are the applicant responsible for the device submission and regulatory documentation.
This description and any FAQs above were generated automatically from registry data and have not been verified by the manufacturer or by deviCERTS. Always check the official registry entry and the manufacturer's instructions for use before relying on them. Sources consulted: Philips - CT Collaboration Live - Philips, Philips Collaboration Live - Philips, Philips - CT Collaboration Live
Authorization Coverage (1 country)
Regulatory Authorizations
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K242329 | Class II | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Philips Healthcare (Suzhou) Co., Ltd.
Sources (1)
- FDA 510(k) K242329 24 fields · synced Sep 21, 2026