{
  "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": "2026-06-01",
    "results": {
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  "results": [
    {
      "third_party_flag": "N",
      "city": "St. Louis",
      "advisory_committee_description": "Cardiovascular",
      "address_1": "4320 Forest Park Ave., Suite 100",
      "address_2": "",
      "statement_or_summary": "Summary",
      "product_code": "PJB",
      "openfda": {
        "device_name": "Catheter Remote Control System",
        "medical_specialty_description": "Cardiovascular",
        "regulation_number": "870.5700",
        "device_class": "2",
        "registration_number": [
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      "zip_code": "63108",
      "applicant": "Stereotaxis, Inc.",
      "decision_date": "2019-10-30",
      "decision_code": "SESE",
      "country_code": "US",
      "device_name": "Niobe® Magnetic Navigation System (MNS) with Navigant Workstation (NWS) and Cardiodri",
      "advisory_committee": "CV",
      "contact": "Kenneth H. Lock",
      "expedited_review_flag": "",
      "k_number": "K192775",
      "state": "MO",
      "date_received": "2019-09-30",
      "review_advisory_committee": "CV",
      "postal_code": "63108",
      "decision_description": "Substantially Equivalent",
      "clearance_type": "Special"
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}