Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

NeuroMatch

K-Number: K250239 · 2025-05-23

ApplicantLVIS Corporation
Decision Date2025-05-23
Product CodeOLX
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NeuroMatch is a medical device manufactured by LVIS Corporation. It received FDA 510(k) clearance on 2025-05-23 under approval number K250239. The device is classified under product code OLX. 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 2025-05-23. It is manufactured by LVIS Corporation. The 510(k) number is K250239.

When was NeuroMatch approved by the FDA?

NeuroMatch received FDA 510(k) clearance on 2025-05-23, under approval number K250239.

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 OLX.

Other Devices by LVIS Corporation

K222450LVIS NeuroMatch K241390NeuroMatch

Related Devices (Code: OLX)

K172858PreOpEpilog K201910EZTrackNeurologic, LLC K210199RICOH MEGRicoh Company, Ltd. K241513SourcererBrain Electrophysiology Laboratory Company, LLC K233985TRIUX™ neo (NM27000N ); MEGreview (SW26241N-B)Megin OY K252565PreOp v3Clouds of Care

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.

↑