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FDA 510(k)

Collaboration Live

K-Number: K201665 · 2020-09-15

ApplicantPhilips Ultrasound, Inc.
Decision Date2020-09-15
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Collaboration Live is a medical device manufactured by Philips Ultrasound, Inc.. It received FDA 510(k) clearance on 2020-09-15 under approval number K201665. 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 Collaboration Live?

Collaboration Live is a medical device that received FDA 510(k) clearance on 2020-09-15. It is manufactured by Philips Ultrasound, Inc.. The 510(k) number is K201665.

When was Collaboration Live approved by the FDA?

Collaboration Live received FDA 510(k) clearance on 2020-09-15, under approval number K201665.

What company makes Collaboration Live?

Collaboration Live is manufactured by Philips Ultrasound, Inc..

What is the FDA product code for Collaboration Live?

The FDA product code for Collaboration Live is LLZ.

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Related Devices (Code: 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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