{
  "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": "Chicopee",
      "advisory_committee_description": "Obstetrics/Gynecology",
      "address_1": "Two Ludlow Park",
      "address_2": "",
      "statement_or_summary": "Summary",
      "product_code": "KXO",
      "openfda": {
        "registration_number": [
          "1921846",
          "1718873",
          "9681860",
          "1423537"
        ],
        "fei_number": [
          "3003491392",
          "1921846",
          "1718873",
          "3001236905"
        ],
        "device_name": "Monitor, Pressure, Intrauterine",
        "medical_specialty_description": "Obstetrics/Gynecology",
        "regulation_number": "884.2700",
        "device_class": "2"
      },
      "zip_code": "01022",
      "applicant": "Ludlow Technical Products",
      "decision_date": "1999-07-08",
      "decision_code": "SESE",
      "country_code": "US",
      "device_name": "SOFTRANS TEMP INTRAUTERINE PRESSURE CATHETER SYSTEM (IUP 5000, SOFTRANS TEMP IUPC)",
      "advisory_committee": "OB",
      "contact": "KATHLEEN M MURPHY",
      "expedited_review_flag": "",
      "k_number": "K991235",
      "state": "MA",
      "date_received": "1999-04-12",
      "review_advisory_committee": "OB",
      "postal_code": "01022",
      "decision_description": "Substantially Equivalent",
      "clearance_type": "Traditional"
    }
  ]
}