{
  "format": "devicerts.device.v1",
  "cite_as": "NeuroMatch, LVIS Corporation. deviCERTS medical device catalogue. https://devicerts.com/devices/neuromatch-olx (data as of 2026-11-15).",
  "source": {
    "canonical_url": "https://devicerts.com/devices/neuromatch-olx",
    "json_url": "https://devicerts.com/devices/neuromatch-olx.json",
    "markdown_url": "https://devicerts.com/devices/neuromatch-olx.md",
    "publisher": "deviCERTS (devicerts.com)",
    "data_sources": [
      {
        "registry": "FDA 510(k)",
        "url": "https://open.fda.gov/apis/device/510k/"
      }
    ],
    "registry_records_last_synced": "2026-10-06",
    "status_as_of": "2026-11-15",
    "license": "CC BY 4.0",
    "license_url": "https://creativecommons.org/licenses/by/4.0/",
    "license_scope": "The deviCERTS layout and text are licensed under CC BY 4.0. Registry data remain under their source terms: U.S. FDA data (openFDA, AccessGUDID) are U.S. public domain; EUDAMED data are subject to the European Commission reuse terms.",
    "attribution": "DevicErts, https://devicerts.com/devices/neuromatch-olx",
    "disclaimer": "Compiled by deviCERTS (devicerts.com) from public medical device registries (EUDAMED, European Commission; U.S. FDA via openFDA; AccessGUDID, U.S. National Library of Medicine). deviCERTS is not an official register and gives no regulatory advice: the record in the registry itself prevails."
  },
  "device": {
    "name": "NeuroMatch",
    "registry_name": "NeuroMatch",
    "url": "https://devicerts.com/devices/neuromatch-olx",
    "manufacturer": {
      "name": "LVIS Corporation",
      "url": "https://devicerts.com/manufacturers/lvis-corporation",
      "country": "United States",
      "country_basis": "FDA 510(k) applicant",
      "fda_registration_country": null
    },
    "status": {
      "state": "active",
      "label": "Active",
      "detail": "United States"
    },
    "classification": [
      {
        "class": "Class II",
        "system": "US FDA"
      }
    ],
    "identifiers": [
      {
        "label": "510(k) Number",
        "values": [
          {
            "value": "K250239",
            "registries": [
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            ]
          }
        ]
      }
    ],
    "product_codes": [
      "OLX"
    ],
    "emdn": [],
    "gmdn": [],
    "description": {
      "text": "NeuroMatch is a source localization software for electroencephalograph or magnetoencephalograph. It is designed to decode brain networks and deliver visualizations of brain activity to assist in neurological diagnosis.\n\nNeuroMatch is supplied as a software platform, available in both traditional and cloud-based SaaS formats. It is intended for use in clinical settings to review and interpret EEG data, supporting quicker and more comprehensive analysis. The device has received FDA 510(k) clearance under product code OLX and regulation number 882.1400.",
      "ai_generated": true,
      "generated_on": "2026-09-27",
      "note": "Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data is the record."
    },
    "noindex": false
  },
  "authorizations": [
    {
      "registry": "510(k)",
      "region": "United States",
      "type": "FDA 510(k)",
      "number": "K250239",
      "number_label": null,
      "device_udi_di": null,
      "date": "2025-05-23",
      "date_kind": "decision",
      "decision_code": "SESE",
      "expires": null,
      "withdrawn": null,
      "status": "Active",
      "status_note": null,
      "derived_from_gudid": false
    }
  ],
  "no_longer_listed_by": [],
  "certificates": [],
  "recalls": [],
  "eu_market_availability": null,
  "properties": [
    {
      "group": "Identifiers",
      "fields": [
        {
          "label": "510(k) Number",
          "values": [
            {
              "value": "K250239",
              "registries": [
                "FDA 510(k)"
              ]
            }
          ]
        },
        {
          "label": "FDA product code",
          "values": [
            {
              "value": "OLX",
              "registries": [
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              ]
            }
          ]
        }
      ]
    },
    {
      "group": "Classification",
      "fields": [
        {
          "label": "Device class",
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            {
              "value": "Class II",
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            }
          ]
        },
        {
          "label": "Regulation",
          "values": [
            {
              "value": "21 CFR Part 882.1400",
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            }
          ]
        },
        {
          "label": "Advisory committee",
          "values": [
            {
              "value": "Neurology",
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          ]
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      ]
    }
  ]
}