{
  "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": "2026-07-27",
    "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": "QRN",
      "openfda": {
        "k_number": [
          "DEN200041",
          "K222112"
        ],
        "registration_number": [
          "3021371724",
          "3008388260",
          "3008574006",
          "3010163695"
        ],
        "fei_number": [
          "3021371724",
          "3008388260",
          "3008574006",
          "3010163695"
        ]
      },
      "review_panel": "RA",
      "medical_specialty": "RA",
      "device_name": "Radiation Therapy Marking Device",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Radiology",
      "device_class": "2",
      "definition": "A radiation therapy marking device is a powered device that transdermally delivers a permanent or temporary colorant to the skin for the purpose of placing marks to guide radiation therapy. This classification does not include devices with reusable or reprocessed needles or devices intended for diagnostic, therapeutic, or aesthetic use or to deliver other products for these uses.",
      "regulation_number": "892.5785",
      "implant_flag": "N",
      "submission_type_id": "1"
    }
  ]
}