{
  "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,
      "limit": 1,
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  "results": [
    {
      "third_party_flag": "N",
      "city": "Vancouver, British Columbia",
      "advisory_committee_description": "Unknown",
      "address_1": "Unit 303, 828 W. 8th Ave.",
      "address_2": "",
      "statement_or_summary": "Summary",
      "product_code": "LXM",
      "openfda": {
        "registration_number": [
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          "2510425",
          "3003418325",
          "2182433",
          "3005205657",
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          "3004904656",
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          "3006315109",
          "2531782",
          "3004620782"
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          "3006315109",
          "3002546832",
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        "device_name": "Manipulator, Plunger-Like Joint",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "U"
      },
      "zip_code": "V5Z 1E2",
      "applicant": "Optima Health Solutions International, Inc.",
      "decision_date": "2006-03-23",
      "decision_code": "SESE",
      "country_code": "CA",
      "device_name": "KHAN KINETIC TREATMENT DEVICE (KKT-M1)",
      "advisory_committee": "",
      "contact": "BRAM  RAMJIAWAN",
      "expedited_review_flag": "",
      "k_number": "K060043",
      "state": "",
      "date_received": "2006-01-06",
      "review_advisory_committee": "PM",
      "postal_code": "V5Z 1E2",
      "decision_description": "Substantially Equivalent",
      "clearance_type": "Traditional"
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}