{
  "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": "SEN",
      "openfda": {
        "k_number": [
          "K233337"
        ],
        "registration_number": [
          "3010887638"
        ],
        "fei_number": [
          "3010887638"
        ]
      },
      "review_panel": "NE",
      "medical_specialty": "NE",
      "device_name": "Biofeedback For Adjunctive Treatment Of Symptoms Associated With Stress And Anxiety",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Neurology",
      "device_class": "2",
      "definition": "A biofeedback device for adjunctive treatment of patient-reported symptoms associated with stress and anxiety is intended to provide feedback to users with patient-reported symptoms associated with stress and anxiety on a physiological measurement as a relaxation treatment for the reduction of stress and anxiety.",
      "regulation_number": "882.5050",
      "implant_flag": "N",
      "submission_type_id": "1"
    }
  ]
}