Collaboration Live
K-Number: K200179 · 2020-02-18
ApplicantPhilips Health Care
Decision Date2020-02-18
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Collaboration Live is a medical device manufactured by Philips Health Care. It received FDA 510(k) clearance on 2020-02-18 under approval number K200179. 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 2020-02-18. It is manufactured by Philips Health Care. The 510(k) number is K200179.
When was Collaboration Live approved by the FDA?
Collaboration Live received FDA 510(k) clearance on 2020-02-18, under approval number K200179.
What company makes Collaboration Live?
Collaboration Live is manufactured by Philips Health Care.
What is the FDA product code for Collaboration Live?
The FDA product code for 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.