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FDA 510(k)

NeuroMatch

K-Number: K241390 · 2024-11-26

ApplicantLVIS Corporation
Decision Date2024-11-26
Product CodeOMB
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NeuroMatch is a medical device manufactured by LVIS Corporation. It received FDA 510(k) clearance on 2024-11-26 under approval number K241390. The device is classified under product code OMB. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NeuroMatch?

NeuroMatch is a medical device that received FDA 510(k) clearance on 2024-11-26. It is manufactured by LVIS Corporation. The 510(k) number is K241390.

When was NeuroMatch approved by the FDA?

NeuroMatch received FDA 510(k) clearance on 2024-11-26, under approval number K241390.

What company makes NeuroMatch?

NeuroMatch is manufactured by LVIS Corporation.

What is the FDA product code for NeuroMatch?

The FDA product code for NeuroMatch is OMB.

Other Devices by LVIS Corporation

K222450LVIS NeuroMatch K250239NeuroMatch

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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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