{
  "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": {
      "skip": 0,
      "limit": 1,
      "total": 2
    }
  },
  "results": [
    {
      "third_party_flag": "N",
      "city": "Nottingham",
      "advisory_committee_description": "Obstetrics/Gynecology",
      "address_1": "Biocity, Pennyfoot St.",
      "address_2": "",
      "statement_or_summary": "Summary",
      "product_code": "OSP",
      "openfda": {
        "device_name": "Uterine Electromyographic Monitor",
        "medical_specialty_description": "Obstetrics/Gynecology",
        "regulation_number": "884.2720",
        "device_class": "2",
        "registration_number": [
          "3007607999",
          "3007048259",
          "1930027",
          "1218950",
          "3016618143",
          "9610816",
          "3007734888",
          "3008729547",
          "3014220748",
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      },
      "zip_code": "NG1 1GF",
      "applicant": "Monica Healthcare, Ltd.",
      "decision_date": "2014-08-27",
      "decision_code": "SESE",
      "country_code": "GB",
      "device_name": "MONICA NOVII WIRELESS PATCH SYSTEM",
      "advisory_committee": "OB",
      "contact": "CARL  BARRATT",
      "expedited_review_flag": "",
      "k_number": "K140862",
      "state": "",
      "date_received": "2014-04-03",
      "review_advisory_committee": "OB",
      "postal_code": "NG1 1GF",
      "decision_description": "Substantially Equivalent",
      "clearance_type": "Traditional"
    }
  ]
}