{
  "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": "2026-10-19",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 2
    }
  },
  "results": [
    {
      "proprietary_name": [
        "Solo Pace Control"
      ],
      "establishment_type": [
        "Develop Specifications But Do Not Manufacture At This Facility",
        "Manufacture Medical Device"
      ],
      "registration": {
        "registration_number": "3035372913",
        "fei_number": "3035372913",
        "status_code": "1",
        "initial_importer_flag": "N",
        "reg_expiry_date_year": "2026",
        "name": "SOLO PACE INC",
        "address_line_1": "7125 Northland Ter N",
        "address_line_2": "",
        "city": "Brooklyn Park",
        "state_code": "MN",
        "iso_country_code": "US",
        "zip_code": "55428",
        "postal_code": "",
        "us_agent": {},
        "owner_operator": {
          "firm_name": "Solo Pace Inc",
          "owner_operator_number": "10092533",
          "official_correspondent": {
            "first_name": "Michelle",
            "middle_initial": "",
            "last_name": "Straight",
            "subaccount_company_name": "",
            "phone_number": "1-612-9407240-x"
          },
          "contact_address": {
            "address_1": "7125 Northland Terrace North",
            "address_2": "",
            "city": "Brooklyn Park",
            "state_code": "MN",
            "state_province": "",
            "iso_country_code": "US",
            "postal_code": "55428"
          }
        }
      },
      "pma_number": "",
      "k_number": "K241781",
      "products": [
        {
          "product_code": "DTE",
          "created_date": "2025-01-17",
          "owner_operator_number": "10092533",
          "exempt": "",
          "openfda": {
            "k_number": [
              "K241781"
            ],
            "device_name": "Pulse-Generator, Pacemaker, External",
            "medical_specialty_description": "Cardiovascular",
            "regulation_number": "870.3600",
            "device_class": "2"
          }
        }
      ]
    }
  ]
}