{
  "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": "2026-06-08",
    "results": {
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  "results": [
    {
      "third_party_flag": "N",
      "city": "Goteborg",
      "advisory_committee_description": "Physical Medicine",
      "address_1": "Kvarnbergsgatan 2",
      "address_2": "",
      "statement_or_summary": "Summary",
      "product_code": "LXJ",
      "openfda": {
        "registration_number": [
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        "device_name": "Interactive Rehabilitation Exercise Devices",
        "medical_specialty_description": "Physical Medicine",
        "regulation_number": "890.5360",
        "device_class": "2"
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      "zip_code": "411 05",
      "applicant": "Qualisys AB",
      "decision_date": "2018-08-02",
      "decision_code": "SESE",
      "country_code": "SE",
      "device_name": "Qualisys Clinical System",
      "advisory_committee": "PM",
      "contact": "Henrik  Wiberg",
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      "k_number": "K171547",
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      "date_received": "2017-05-26",
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      "decision_description": "Substantially Equivalent",
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}