{
  "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": "Oak Ridge",
      "advisory_committee_description": "Hematology",
      "address_1": "107 Meco Ln.",
      "address_2": "",
      "statement_or_summary": "Summary",
      "product_code": "JWO",
      "openfda": {
        "device_name": "Device, Blood Volume Measuring",
        "medical_specialty_description": "Hematology",
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      "applicant": "Daxor Corporation",
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      "decision_code": "SESE",
      "country_code": "US",
      "device_name": "Blood Volume Analyzer (200)",
      "advisory_committee": "HE",
      "contact": "Jonathan  Feldschuh",
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      "k_number": "K251087",
      "state": "TN",
      "date_received": "2025-04-09",
      "review_advisory_committee": "HE",
      "postal_code": "37830",
      "decision_description": "Substantially Equivalent",
      "clearance_type": "Traditional"
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}