{
  "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": 1
    }
  },
  "results": [
    {
      "third_party_flag": "N",
      "life_sustain_support_flag": "N",
      "gmp_exempt_flag": "N",
      "summary_malfunction_reporting": "Ineligible",
      "product_code": "QWD",
      "openfda": {
        "k_number": [
          "DEN220059"
        ],
        "registration_number": [
          "3025729280",
          "9710609",
          "3032776111"
        ],
        "fei_number": [
          "3003202721",
          "3025729280",
          "3032776111"
        ]
      },
      "review_panel": "NE",
      "medical_specialty": "NE",
      "device_name": "Stimulator, Nerve, For Restless Legs Syndrome",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Neurology",
      "device_class": "2",
      "definition": "An external lower extremity nerve stimulator for Restless Legs Syndrome is a prescription device that uses external electrical stimulators and cutaneous electrodes to stimulate nerves in the lower extremity (e.g.,peroneal nerves) and evoke tonic, sustained muscle activation in the legs to reduce the symptoms of Restless Legs Syndrome.",
      "regulation_number": "882.5887",
      "implant_flag": "N",
      "submission_type_id": "1"
    }
  ]
}