{
  "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": "2026-10-12",
    "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": "QHJ",
      "openfda": {
        "pma_number": [
          "P160048"
        ],
        "registration_number": [
          "3009810261",
          "3004530184",
          "3012761544",
          "2133810",
          "9614698",
          "3003335547",
          "2183744",
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      },
      "review_panel": "CH",
      "medical_specialty": "",
      "device_name": "Sensor, Glucose, Implanted, Non-Adjunctive Use",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Unknown",
      "device_class": "3",
      "definition": "A non-adjunctive implanted glucose sensor is intended to determine glucose   levels, and the direction and rate of change of glucose levels in people with   diabetes. The device is indicated to replace information obtained from standard   blood glucose monitoring devices to make diabetes-related treatment decisions. The device also provides historical glucose information, facilitating long-term therapy adjustments.",
      "regulation_number": "",
      "implant_flag": "Y",
      "submission_type_id": "2"
    }
  ]
}