{
  "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": "2026-07-27",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 2
    }
  },
  "results": [
    {
      "third_party_flag": "N",
      "city": "Germantown",
      "advisory_committee_description": "Ear, Nose, Throat",
      "address_1": "W175 N11081 Stonewood Dr.",
      "address_2": "",
      "statement_or_summary": "",
      "product_code": "PKA",
      "openfda": {
        "device_name": "External Upper Esophageal Sphincter (Ues) Compression Device",
        "medical_specialty_description": "Ear, Nose, Throat",
        "regulation_number": "874.5900",
        "device_class": "2",
        "registration_number": [
          "3039167637"
        ],
        "fei_number": [
          "3039167637"
        ]
      },
      "zip_code": "53022",
      "applicant": "Somna Therapeutics, LLC",
      "decision_date": "2015-03-06",
      "decision_code": "DENG",
      "country_code": "US",
      "device_name": "REZA BAND(TM) UPPER ESOPHAGEAL (UES) SPHINCTER ASSIST DEVICE",
      "advisory_committee": "EN",
      "contact": "James S. Miller",
      "expedited_review_flag": "",
      "k_number": "DEN130046",
      "state": "WI",
      "date_received": "2013-11-14",
      "review_advisory_committee": "EN",
      "postal_code": "53022",
      "decision_description": "Unknown",
      "clearance_type": "Direct"
    }
  ]
}