{
  "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": "2026-08-03",
    "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": "OLM",
      "openfda": {
        "registration_number": [
          "3009380063",
          "2649622",
          "3004593495",
          "2183744",
          "3004209178",
          "3018094310",
          "2135338",
          "2182207"
        ],
        "fei_number": [
          "3009380063",
          "3004369318",
          "2649622",
          "3004593495",
          "3005700659",
          "2183744",
          "3018094310",
          "2182207"
        ]
      },
      "review_panel": "NE",
      "medical_specialty": "",
      "device_name": "Deep Brain Stimulator For Obsessive Compulsive Disorder (Ocd)",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Unknown",
      "device_class": "f",
      "definition": "The device is indicated for bilateral stimulation of the anterior limb of the internal capsule, this device is indicated as an adjunct to medications and as an alternative to anterior capsulotomy for treatment of chronic, severe, treatment-resistant Obsessive Compulsive Disorder (OCD) in adult patients who have failed at least three Selective Serotonin Reuptake Inhibitors (SSRIs).",
      "regulation_number": "",
      "implant_flag": "Y",
      "submission_type_id": "6"
    }
  ]
}