{
  "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": {
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  "results": [
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      "third_party_flag": "N",
      "city": "Askim",
      "advisory_committee_description": "Ear, Nose, Throat",
      "address_1": "Datavagen 37 B",
      "address_2": "",
      "statement_or_summary": "Summary",
      "product_code": "MAH",
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        "medical_specialty_description": "Ear, Nose, Throat",
        "regulation_number": "874.3302",
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      "zip_code": "436 32",
      "applicant": "Oticon Medical AB",
      "decision_date": "2016-01-22",
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      "device_name": "Ponto Bone Anchored Hearing System",
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}