{
  "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": "2026-09-07",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "proprietary_name": [
        "Intellisep Cartridge"
      ],
      "establishment_type": [
        "Manufacture Medical Device for Another Party (Contract Manufacturer)"
      ],
      "registration": {
        "registration_number": "3005288662",
        "fei_number": "3005288662",
        "status_code": "1",
        "initial_importer_flag": "N",
        "reg_expiry_date_year": "2026",
        "name": "Westec Plastics Corporation",
        "address_line_1": "6757 Las Positas Rd Ste A",
        "address_line_2": "",
        "city": "Livermore",
        "state_code": "CA",
        "iso_country_code": "US",
        "zip_code": "94551",
        "postal_code": "",
        "us_agent": {},
        "owner_operator": {
          "firm_name": "QA Manager",
          "owner_operator_number": "10091936",
          "official_correspondent": {
            "first_name": "Lucero",
            "middle_initial": "",
            "last_name": "Castro",
            "subaccount_company_name": "",
            "phone_number": "x-925-4543400-118"
          },
          "contact_address": {
            "address_1": "6757 Las Positas Rd.",
            "address_2": "",
            "city": "Livermore",
            "state_code": "CA",
            "state_province": "",
            "iso_country_code": "US",
            "postal_code": "94550"
          }
        }
      },
      "pma_number": "",
      "k_number": "",
      "products": [
        {
          "product_code": "QUT",
          "created_date": "2024-11-18",
          "owner_operator_number": "10091936",
          "exempt": "",
          "openfda": {
            "device_name": "Deformability Cytometry For Sepsis Risk Assessment",
            "medical_specialty_description": "Microbiology",
            "regulation_number": "866.3215",
            "device_class": "2"
          }
        }
      ]
    }
  ]
}