{
  "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,
      "total": 4
    }
  },
  "results": [
    {
      "third_party_flag": "N",
      "city": "Sunnyvale",
      "advisory_committee_description": "Cardiovascular",
      "address_1": "271 Gibraltar Dr.",
      "address_2": "",
      "statement_or_summary": "Summary",
      "product_code": "OTD",
      "openfda": {
        "registration_number": [
          "3002807314",
          "9612164",
          "2953200",
          "2011171",
          "3009380063"
        ],
        "fei_number": [
          "3002807314",
          "3002806434",
          "2011171",
          "3001452571",
          "3009380063"
        ],
        "device_name": "Endovascular Suturing System",
        "medical_specialty_description": "Cardiovascular",
        "regulation_number": "870.3460",
        "device_class": "2"
      },
      "zip_code": "94089",
      "applicant": "Aptus Endosystems, Inc.",
      "decision_date": "2014-02-06",
      "decision_code": "SESE",
      "country_code": "US",
      "device_name": "APTUS HELI-FX GUIDE - 22CM DEFLECTABLE LENGTH; APTUS HELI-FX GUIDE - 28CM DEFLECTABLE LENGTH; APTUS HELI-FX APPLIER WITH",
      "advisory_committee": "CV",
      "contact": "BURT  GOODSON",
      "expedited_review_flag": "",
      "k_number": "K140036",
      "state": "CA",
      "date_received": "2014-01-07",
      "review_advisory_committee": "CV",
      "postal_code": "94089",
      "decision_description": "Substantially Equivalent",
      "clearance_type": "Special"
    }
  ]
}