{
  "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": "Y",
      "city": "Finning, Bavaria",
      "advisory_committee_description": "General Hospital",
      "address_1": "Lerchenberg 20",
      "address_2": "",
      "statement_or_summary": "Statement",
      "product_code": "FLN",
      "openfda": {
        "registration_number": [
          "1643264",
          "3003604053",
          "2030624"
        ],
        "fei_number": [
          "1643264",
          "3003604053",
          "3000206435"
        ],
        "device_name": "Monitor, Electric For Gravity Flow Infusion Systems",
        "medical_specialty_description": "General Hospital",
        "regulation_number": "880.2420",
        "device_class": "2"
      },
      "zip_code": "86923",
      "applicant": "Em-Tec GmbH",
      "decision_date": "2008-04-17",
      "decision_code": "SESE",
      "country_code": "DE",
      "device_name": "LOW FLUID ALARM",
      "advisory_committee": "HO",
      "contact": "BERNHARD  BRAND",
      "expedited_review_flag": "",
      "k_number": "K080704",
      "state": "",
      "date_received": "2008-03-12",
      "review_advisory_committee": "HO",
      "postal_code": "86923",
      "decision_description": "Substantially Equivalent",
      "clearance_type": "Abbreviated"
    }
  ]
}