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FDA 510(k)

The Multimodality Advanced Vessel Analysis

K-Number: K203216 · 2020-11-25

ApplicantPhilips Medical Systems Nederland B.V.
Decision Date2020-11-25
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

The Multimodality Advanced Vessel Analysis is a medical device manufactured by Philips Medical Systems Nederland B.V.. It received FDA 510(k) clearance on 2020-11-25 under approval number K203216. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the The Multimodality Advanced Vessel Analysis?

The Multimodality Advanced Vessel Analysis is a medical device that received FDA 510(k) clearance on 2020-11-25. It is manufactured by Philips Medical Systems Nederland B.V.. The 510(k) number is K203216.

When was The Multimodality Advanced Vessel Analysis approved by the FDA?

The Multimodality Advanced Vessel Analysis received FDA 510(k) clearance on 2020-11-25, under approval number K203216.

What company makes The Multimodality Advanced Vessel Analysis?

The Multimodality Advanced Vessel Analysis is manufactured by Philips Medical Systems Nederland B.V..

What is the FDA product code for The Multimodality Advanced Vessel Analysis?

The FDA product code for The Multimodality Advanced Vessel Analysis is JAK.

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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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