{
  "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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      "third_party_flag": "N",
      "city": "Birmingham",
      "advisory_committee_description": "Cardiovascular",
      "address_1": "434 Industrial Ln.",
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      "statement_or_summary": "Summary",
      "product_code": "NMD",
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        "medical_specialty_description": "Cardiovascular",
        "regulation_number": "870.2700",
        "device_class": "2"
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      "zip_code": "35211",
      "applicant": "Midwest Reprocessing Center, LLC",
      "decision_date": "2011-06-08",
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      "device_name": "MIDWEST REPROCESSING CENTER REPROCESSED LNCS SESSORS; MIDWEST REPROCESSING CENTER REPROCESSED OXIMAX SENSORS; MIDWEST RE",
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      "k_number": "K111007",
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      "decision_description": "Substantially Equivalent",
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}