{
  "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": [
    {
      "third_party_flag": "N",
      "city": "Newcastle Upon Tyne",
      "advisory_committee_description": "Hematology",
      "address_1": "Balliol Business Park W.",
      "address_2": "Benton Ln.",
      "statement_or_summary": "Summary",
      "product_code": "MXZ",
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        "medical_specialty_description": "Hematology",
        "regulation_number": "864.1860",
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      },
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      "applicant": "Leica Biosystems Newcastle, Ltd.",
      "decision_date": "2020-03-06",
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      "country_code": "GB",
      "device_name": "BOND Ready-to-Use Primary Antibody Progesterone Receptor (16), Novocastra Liquid Mouse Monoclonal Antibody Progesterone Receptor Clone 16 (Concentrated Liquid Antibody Format).",
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      "decision_description": "Substantially Equivalent",
      "clearance_type": "Traditional"
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  ]
}