{
  "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": "SIM",
      "openfda": {
        "k_number": [
          "DEN250034"
        ],
        "registration_number": [
          "3023620966"
        ],
        "fei_number": [
          "3023620966"
        ]
      },
      "review_panel": "OB",
      "medical_specialty": "OB",
      "device_name": "Gynecologic Power Morcellator And Containment System",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Obstetrics/Gynecology",
      "device_class": "2",
      "definition": "A gynecologic power morcellator and containment system is a prescription device consisting of an integrated power morcellator and a containment method that are intended to contain, reduce and remove gynecologic tissue that is not suspected to contain malignancy during minimally invasive surgery.",
      "regulation_number": "884.4075",
      "implant_flag": "N",
      "submission_type_id": "1"
    }
  ]
}