{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-06-01",
    "results": {
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  "results": [
    {
      "third_party_flag": "N",
      "city": "Lake Bluff",
      "advisory_committee_description": "Neurology",
      "address_1": "910 Sherwood Dr., Unit 17",
      "address_2": "",
      "statement_or_summary": "Summary",
      "product_code": "QGH",
      "openfda": {
        "device_name": "Electroconvulsive Therapy Device For Catatonia, Major Depressive Disorder, And Bipolar Disorder",
        "medical_specialty_description": "Neurology",
        "regulation_number": "882.5940",
        "device_class": "2",
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          "3023869663",
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          "3023869663",
          "1420295"
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      "applicant": "Somatics, Inc.",
      "decision_date": "1995-10-26",
      "decision_code": "SESE",
      "country_code": "US",
      "device_name": "THYMATRON 2000 ELECTROCONVULSIVE SYSTEM",
      "advisory_committee": "NE",
      "contact": "RICHARD  ABRAMS",
      "expedited_review_flag": "",
      "k_number": "K945120",
      "state": "IL",
      "date_received": "1994-10-19",
      "review_advisory_committee": "NE",
      "postal_code": "60044",
      "decision_description": "Substantially Equivalent",
      "clearance_type": "Traditional"
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}