NeuroMatch— 510(k) K250239

Substantially Equivalent

LVIS Corporation

FDA 510(k) clearance K250239 for NeuroMatch, Substantially Equivalent on 2025-05-23. Applicant: LVIS Corporation.

Clearance details

Applicant: LVIS Corporation
Product code: Code OLX
Advisory panel: Neurology
Date received: 2025-01-27
Decision date: 2025-05-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Palo Alto, CA, US

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