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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 the device name listed in this FDA 510(k) record. The listed applicant is Neurocareai, Inc.. It received FDA 510(k) clearance on 2024-11-07 under 510(k) 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. The listed applicant is Neurocareai, Inc.. The 510(k) number is K241719.

When did NeuroICH receive FDA 510(k) clearance?

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

Who is the listed applicant for NeuroICH?

The FDA 510(k) record lists Neurocareai, Inc. as the applicant. This does not by itself establish the device manufacturer.

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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