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FDA 510(k)

CT Collaboration Live

K-Number: K242329 · 2024-11-18

ApplicantPhilips Healthcare (Suzhou) Co., Ltd.
Decision Date2024-11-18
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CT Collaboration Live is a medical device manufactured by Philips Healthcare (Suzhou) Co., Ltd.. It received FDA 510(k) clearance on 2024-11-18 under approval number K242329. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

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. It is manufactured by Philips Healthcare (Suzhou) Co., Ltd.. The 510(k) number is K242329.

When was CT Collaboration Live approved by the FDA?

CT Collaboration Live received FDA 510(k) clearance on 2024-11-18, under approval number K242329.

What company makes CT Collaboration Live?

CT Collaboration Live is manufactured by Philips Healthcare (Suzhou) Co., Ltd..

What is the FDA product code for CT Collaboration Live?

The FDA product code for CT Collaboration Live is LLZ.

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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.

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