{
  "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": "Drachten",
      "advisory_committee_description": "Microbiology",
      "address_1": "Marconilaan 6",
      "address_2": "",
      "statement_or_summary": "Summary",
      "product_code": "QQY",
      "openfda": {
        "device_name": "Culture Plate Imaging System For Qualitative Assessment Of Resistant Organisms",
        "medical_specialty_description": "Microbiology",
        "regulation_number": "866.2190",
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          "1119779",
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      "applicant": "Bd Kiestra B.V.",
      "decision_date": "2023-05-04",
      "decision_code": "SESE",
      "country_code": "NL",
      "device_name": "BD Kiestra Methicillin-resistant Staphylococcus aureus (MRSA) Application,  BD Kiestra MRSA App",
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      "k_number": "K213280",
      "state": "",
      "date_received": "2021-10-01",
      "review_advisory_committee": "MI",
      "postal_code": "9207 JC",
      "decision_description": "Substantially Equivalent",
      "clearance_type": "Traditional"
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}