{
  "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": "2026-04-13",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "third_party_flag": "N",
      "city": "Buffalo",
      "advisory_committee_description": "Obstetrics/Gynecology",
      "address_1": "P.O. Box 1274",
      "address_2": "189 Van Rensselaer St.",
      "statement_or_summary": "Statement",
      "product_code": "KXO",
      "openfda": {
        "device_name": "Monitor, Pressure, Intrauterine",
        "medical_specialty_description": "Obstetrics/Gynecology",
        "regulation_number": "884.2700",
        "device_class": "2",
        "registration_number": [
          "1423537",
          "1921846",
          "9681860",
          "1718873"
        ],
        "fei_number": [
          "3003491392",
          "1921846",
          "1718873",
          "3001236905"
        ]
      },
      "zip_code": "14240",
      "applicant": "Graphic Controls Corp.",
      "decision_date": "1995-05-25",
      "decision_code": "SESE",
      "country_code": "US",
      "device_name": "LIFETRACE INTRAUTERINE PRESSURE CATHETER IUP 3000",
      "advisory_committee": "OB",
      "contact": "IGNATY  GUSAKOV",
      "expedited_review_flag": "",
      "k_number": "K950708",
      "state": "NY",
      "date_received": "1995-02-13",
      "review_advisory_committee": "OB",
      "postal_code": "14240",
      "decision_description": "Substantially Equivalent",
      "clearance_type": "Traditional"
    }
  ]
}