{
  "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": "Eden Prairie",
      "advisory_committee_description": "General, Plastic Surgery",
      "address_1": "10393 W. 70th St.",
      "address_2": "",
      "statement_or_summary": "Summary",
      "product_code": "MSA",
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        "medical_specialty_description": "General, Plastic Surgery",
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      "decision_date": "2002-01-31",
      "decision_code": "SESE",
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      "device_name": "MODIFICATION TO AUGUSTINE MEDICAL WOUND CARE SYSTEM, MODEL 68XXX",
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      "contact": "SCOTT D AUGUSTINE",
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      "k_number": "K020077",
      "state": "MN",
      "date_received": "2002-01-09",
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      "decision_description": "Substantially Equivalent",
      "clearance_type": "Special"
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}