{
  "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": "2026-06-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "third_party_flag": "N",
      "city": "20101 Turku",
      "advisory_committee_description": "Microbiology",
      "address_1": "P.O. Box 425",
      "address_2": "",
      "statement_or_summary": "",
      "product_code": "LQN",
      "openfda": {
        "device_name": "Latex Agglutination Assay, Rubella",
        "medical_specialty_description": "Microbiology",
        "regulation_number": "866.3510",
        "device_class": "2",
        "registration_number": [
          "2029372",
          "1641328"
        ],
        "fei_number": [
          "1000306617",
          "1641328"
        ]
      },
      "zip_code": "",
      "applicant": "Orion Corp.",
      "decision_date": "1986-06-04",
      "decision_code": "SESE",
      "country_code": "FI",
      "device_name": "RUBALEX (REVISED VERSION)",
      "advisory_committee": "MI",
      "contact": "TIMO  RAINES",
      "expedited_review_flag": "",
      "k_number": "K861881",
      "state": "",
      "date_received": "1986-05-08",
      "review_advisory_committee": "MI",
      "postal_code": "",
      "decision_description": "Substantially Equivalent",
      "clearance_type": "Traditional"
    }
  ]
}