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FDA 510(k)

NeuroICH

K-Number: K241719 · 2024-11-07

ApplicantNeurocareai, Inc.
Decision Date2024-11-07
Product CodeQAS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

NeuroICH is a medical device manufactured by Neurocareai, Inc.. It received FDA 510(k) clearance on 2024-11-07 under approval number K241719. The device is classified under product code QAS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NeuroICH?

NeuroICH is a medical device that received FDA 510(k) clearance on 2024-11-07. It is manufactured by Neurocareai, Inc.. The 510(k) number is K241719.

When was NeuroICH approved by the FDA?

NeuroICH received FDA 510(k) clearance on 2024-11-07, under approval number K241719.

What company makes NeuroICH?

NeuroICH is manufactured by Neurocareai, Inc..

What is the FDA product code for NeuroICH?

The FDA product code for NeuroICH is QAS.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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