{
  "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": "2026-07-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "third_party_flag": "N",
      "city": "Toronto, Ontario",
      "advisory_committee_description": "Gastroenterology, Urology",
      "address_1": "6 Dornfell St.",
      "address_2": "",
      "statement_or_summary": "Statement",
      "product_code": "FFX",
      "openfda": {
        "device_name": "System, Gastrointestinal Motility (Electrical)",
        "medical_specialty_description": "Gastroenterology, Urology",
        "regulation_number": "876.1725",
        "device_class": "2",
        "registration_number": [
          "3007662958",
          "3018094310",
          "3012302888",
          "3008361498",
          "3016544248",
          "2023374",
          "9611668",
          "3017448360",
          "3016854619",
          "3035451914",
          "1836324",
          "3010082909",
          "9710107",
          "3009106214",
          "1126271",
          "1119033",
          "3015198783",
          "3010381606",
          "3004904811",
          "3013973539",
          "3002806603",
          "3011790297",
          "1123137",
          "3008717264",
          "3009445917",
          "9681384",
          "3008414621",
          "8020893",
          "3012480535",
          "3002821211",
          "9611896"
        ],
        "fei_number": [
          "3007662958",
          "3018094310",
          "3012302888",
          "3009293069",
          "3008361498",
          "3016544248",
          "2023374",
          "3017448360",
          "3016854619",
          "3035451914",
          "3010082909",
          "3002807850",
          "3009106214",
          "1119033",
          "3015198783",
          "3010381606",
          "3002807135",
          "3004904811",
          "3013973539",
          "1000123180",
          "3002806603",
          "3002998595",
          "3011790297",
          "3003348376",
          "1000263641",
          "3008717264",
          "3002807626",
          "3002957361",
          "3008414621",
          "3012480535",
          "3002821211"
        ]
      },
      "zip_code": "M2R 2Y6",
      "applicant": "G & J Electronics, Inc.",
      "decision_date": "1999-06-04",
      "decision_code": "SESE",
      "country_code": "CA",
      "device_name": "GASTRIC AND RECTAL CATHETERS",
      "advisory_committee": "GU",
      "contact": "SAM  JUNDLER",
      "expedited_review_flag": "",
      "k_number": "K973844",
      "state": "",
      "date_received": "1997-10-08",
      "review_advisory_committee": "GU",
      "postal_code": "M2R 2Y6",
      "decision_description": "Substantially Equivalent",
      "clearance_type": "Traditional"
    }
  ]
}