{
  "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": "2026-11-02",
    "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": "MUZ",
      "openfda": {
        "pma_number": [
          "P970003"
        ],
        "registration_number": [
          "1644487"
        ],
        "fei_number": [
          "1000117004"
        ]
      },
      "review_panel": "NE",
      "medical_specialty": "",
      "device_name": "Stimulator, Autonomic Nerve, Implanted (Depression)",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Unknown",
      "device_class": "3",
      "definition": "The device is indicated for the adjunctive long-term treatment of chronic or recurrent depression for patients 18 years of age or older who are experiencing a major depressive episode and have not had an adequate response to four or more adequate antidepressant treatments.",
      "regulation_number": "",
      "implant_flag": "Y",
      "submission_type_id": "2"
    }
  ]
}