{
  "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": {
      "skip": 0,
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  "results": [
    {
      "third_party_flag": "N",
      "city": "Ontario M5t 1x4",
      "advisory_committee_description": "Clinical Toxicology",
      "address_1": "179 John St., 4th Floor ,",
      "address_2": "Toronto",
      "statement_or_summary": "",
      "product_code": "LCS",
      "openfda": {
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        "registration_number": [
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        "fei_number": [
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      "applicant": "Cyberfluor, Inc.",
      "decision_date": "1989-01-17",
      "decision_code": "SESE",
      "country_code": "CA",
      "device_name": "FIAGEN DIGOXIN TIME-RESOLVED FLUOROIMMUNOASSAY KIT",
      "advisory_committee": "TX",
      "contact": "JAMES  CLELLAND",
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      "k_number": "K884707",
      "state": "",
      "date_received": "1988-11-09",
      "review_advisory_committee": "CH",
      "postal_code": "",
      "decision_description": "Substantially Equivalent",
      "clearance_type": "Traditional"
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}