CT Collaboration Live
K-Number: K242329 · 2024-11-18
Device Summary
Frequently Asked Questions
What is the CT Collaboration Live?
CT Collaboration Live is a medical device that received FDA 510(k) clearance on 2024-11-18. The listed applicant is Philips Healthcare (Suzhou) Co., Ltd.. The 510(k) number is K242329.
When did CT Collaboration Live receive FDA 510(k) clearance?
CT Collaboration Live received FDA 510(k) clearance on 2024-11-18, under 510(k) number K242329.
Who is the listed applicant for CT Collaboration Live?
The FDA 510(k) record lists Philips Healthcare (Suzhou) Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CT Collaboration Live?
The FDA product code for CT Collaboration Live is LLZ.
Other records listing Philips Healthcare (Suzhou) Co., Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: LLZ)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.