{
  "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": "2026-10-12",
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      "applicant": "Medtronic Cryocath, LP",
      "street_1": "8200 Coral Sea St.",
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      "city": "Mounds View",
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      "supplement_reason": "Process Change - Manufacturer/Sterilizer/Packager/Supplier",
      "expedited_review_flag": "N",
      "date_received": "2023-12-11",
      "decision_date": "2024-01-08",
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      "decision_code": "OK30",
      "ao_statement": "a new mold for the rear strain relief component used in manufacturing Arctic Front Advance and Arctic Front Advance Pro and the rear strain relief proximal component used in manufacturing Freezer, Freezer Xtra, and Freezer MAX",
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