{
  "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",
      "city": "Englewood",
      "advisory_committee_description": "Cardiovascular",
      "address_1": "12741 E. Caley Ave.",
      "address_2": "Suite 128",
      "statement_or_summary": "",
      "product_code": "DRO",
      "openfda": {
        "registration_number": [
          "3013826848",
          "1921846",
          "3015876",
          "3010703925",
          "3003832357",
          "8030978",
          "3015997711",
          "1930027",
          "1423537",
          "3004906872",
          "3003493679",
          "3000126629",
          "1219103",
          "3003800159",
          "3007029079",
          "1220908",
          "3012104670",
          "3010317211",
          "3008717264",
          "3009077524",
          "3017422354"
        ],
        "fei_number": [
          "3002808182",
          "3013826848",
          "1921846",
          "3015876",
          "3010703925",
          "3003832357",
          "3015997711",
          "1930027",
          "3004906872",
          "3003493679",
          "1000148701",
          "3000126629",
          "3003800159",
          "3007029079",
          "1220908",
          "3012104670",
          "3010317211",
          "3001236905",
          "3008717264",
          "3009077524",
          "3017422354"
        ],
        "device_name": "Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)",
        "medical_specialty_description": "Cardiovascular",
        "regulation_number": "870.5550",
        "device_class": "2"
      },
      "zip_code": "80111",
      "applicant": "Micromedical Devices, Inc.",
      "decision_date": "1985-06-19",
      "decision_code": "SESE",
      "country_code": "US",
      "device_name": "MDI 2000 - PULSE GENERATOR",
      "advisory_committee": "CV",
      "contact": "KAREN  MURPHY",
      "expedited_review_flag": "",
      "k_number": "K850791",
      "state": "CO",
      "date_received": "1985-02-26",
      "review_advisory_committee": "CV",
      "postal_code": "80111",
      "decision_description": "Substantially Equivalent",
      "clearance_type": "Traditional"
    }
  ]
}