{
  "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": "San Jose",
      "advisory_committee_description": "Microbiology",
      "address_1": "2050 Concourse Dr.",
      "address_2": "",
      "statement_or_summary": "",
      "product_code": "GRE",
      "openfda": {
        "registration_number": [
          "1181055",
          "3004973408",
          "1419968"
        ],
        "fei_number": [
          "1181055",
          "3004973408",
          "1419968"
        ],
        "device_name": "Antiserum, Fluorescent, Rubeola",
        "medical_specialty_description": "Microbiology",
        "regulation_number": "866.3520",
        "device_class": "1"
      },
      "zip_code": "95131",
      "applicant": "Idt, A Division of Whittaker M.A. Bioproducts",
      "decision_date": "1985-10-22",
      "decision_code": "SESE",
      "country_code": "US",
      "device_name": "FIAX TEST KIT FOR MEASLES-G ANTIBODIES FLYORESCENT",
      "advisory_committee": "MI",
      "contact": "LOUISE  HARRIS",
      "expedited_review_flag": "",
      "k_number": "K853067",
      "state": "CA",
      "date_received": "1985-07-22",
      "review_advisory_committee": "MI",
      "postal_code": "95131",
      "decision_description": "Substantially Equivalent",
      "clearance_type": "Traditional"
    }
  ]
}