{
  "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": "2026-07-27",
    "results": {
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    {
      "third_party_flag": "N",
      "city": "Woburn",
      "advisory_committee_description": "General Hospital",
      "address_1": "300 Tradecenter, Suite 5400",
      "address_2": "",
      "statement_or_summary": "Summary",
      "product_code": "OKL",
      "openfda": {
        "device_name": "Intravascular Administration Set, Automated Air Removal System",
        "medical_specialty_description": "General Hospital",
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      "applicant": "Clearline MD",
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      "decision_code": "SESE",
      "country_code": "US",
      "device_name": "ClearLine IV",
      "advisory_committee": "HO",
      "contact": "Rick  Romeo",
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      "k_number": "K171954",
      "state": "MA",
      "date_received": "2017-06-29",
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      "postal_code": "01801",
      "decision_description": "Substantially Equivalent",
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}