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FDA 510(k)

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 the device name listed in this FDA 510(k) record. The listed applicant is Philips Health Care. It received FDA 510(k) clearance on 2020-02-18 under 510(k) 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. The listed applicant is Philips Health Care. The 510(k) number is K200179.

When did Collaboration Live receive FDA 510(k) clearance?

Collaboration Live received FDA 510(k) clearance on 2020-02-18, under 510(k) number K200179.

Who is the listed applicant for Collaboration Live?

The FDA 510(k) record lists Philips Health Care as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Collaboration Live?

The FDA product code for Collaboration Live is LLZ.

Other records listing Philips Health Care as applicant

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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.

K262449AdvaViewADVAHEALTH SOLUTIONS, LLCK261916NeuroQuant PETCortechs Labs, Inc.K260936RadioViewAINeurocareai, Inc. (Dba Savelife.Ai)K260588Cleerly LABSCleerly, Inc.K262462TheraSphere 360™ Y-90 Management PlatformBoston Scientific CorporationK262143ImageGrid StreamVueCandelis, Inc.

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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