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FDA 510(k)

icobrain

K-Number: K180326 · 2018-03-08

ApplicantIcometrix
Decision Date2018-03-08
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

icobrain is a medical device manufactured by Icometrix. It received FDA 510(k) clearance on 2018-03-08 under approval number K180326. 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 icobrain?

icobrain is a medical device that received FDA 510(k) clearance on 2018-03-08. It is manufactured by Icometrix. The 510(k) number is K180326.

When was icobrain approved by the FDA?

icobrain received FDA 510(k) clearance on 2018-03-08, under approval number K180326.

What company makes icobrain?

icobrain is manufactured by Icometrix.

What is the FDA product code for icobrain?

The FDA product code for icobrain is LLZ.

Other Devices by Icometrix

K161148icobrain

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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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