{
  "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": 1
    }
  },
  "results": [
    {
      "third_party_flag": "N",
      "life_sustain_support_flag": "N",
      "gmp_exempt_flag": "N",
      "summary_malfunction_reporting": "Eligible",
      "product_code": "PKA",
      "openfda": {
        "k_number": [
          "K173934",
          "DEN130046"
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        "registration_number": [
          "3039167637"
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        "fei_number": [
          "3039167637"
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      },
      "review_panel": "EN",
      "medical_specialty": "EN",
      "device_name": "External Upper Esophageal Sphincter (Ues) Compression Device",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Ear, Nose, Throat",
      "device_class": "2",
      "definition": "The external UES compression device is intended to reduce the symptoms of laryngopharyngeal reflux (LPR) disease by reducing the regurgitation of stomach contents from passing through the upper esophageal sphincter.",
      "regulation_number": "874.5900",
      "implant_flag": "N",
      "submission_type_id": "1"
    }
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}