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FDA 510(k)

INNOLUX RIC

K-Number: K162344 · 2016-12-20

ApplicantInnolux Corporation
Decision Date2016-12-20
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

INNOLUX RIC is a medical device manufactured by Innolux Corporation. It received FDA 510(k) clearance on 2016-12-20 under approval number K162344. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INNOLUX RIC?

INNOLUX RIC is a medical device that received FDA 510(k) clearance on 2016-12-20. It is manufactured by Innolux Corporation. The 510(k) number is K162344.

When was INNOLUX RIC approved by the FDA?

INNOLUX RIC received FDA 510(k) clearance on 2016-12-20, under approval number K162344.

What company makes INNOLUX RIC?

INNOLUX RIC is manufactured by Innolux Corporation.

What is the FDA product code for INNOLUX RIC?

The FDA product code for INNOLUX RIC is MQB.

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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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