{
  "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": "Waukesha",
      "advisory_committee_description": "General Hospital",
      "address_1": "W226n918 Northmound Dr., Suite 300",
      "address_2": "",
      "statement_or_summary": "Summary",
      "product_code": "QXJ",
      "openfda": {
        "device_name": "Whole Room Microbial Reduction Device",
        "medical_specialty_description": "General Hospital",
        "regulation_number": "880.6510",
        "device_class": "2",
        "registration_number": [
          "3014531752",
          "3013869012"
        ],
        "fei_number": [
          "3014531752",
          "3013869012"
        ]
      },
      "zip_code": "53186",
      "applicant": "Preventamed Technologies, Inc. Dba Surfacide Manufacturing",
      "decision_date": "2025-05-27",
      "decision_code": "SESE",
      "country_code": "US",
      "device_name": "Helios+ UV-C System",
      "advisory_committee": "HO",
      "contact": "Jeffry  Veenhuis",
      "expedited_review_flag": "",
      "k_number": "K242604",
      "state": "WI",
      "date_received": "2024-08-30",
      "review_advisory_committee": "HO",
      "postal_code": "53186",
      "decision_description": "Substantially Equivalent",
      "clearance_type": "Traditional"
    }
  ]
}