{
  "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",
      "life_sustain_support_flag": "N",
      "gmp_exempt_flag": "N",
      "summary_malfunction_reporting": "Ineligible",
      "product_code": "SBO",
      "openfda": {
        "k_number": [
          "K233096"
        ],
        "registration_number": [
          "3039200836",
          "3017415521",
          "1424774"
        ],
        "fei_number": [
          "3039200836",
          "3017415521",
          "3003473196"
        ]
      },
      "review_panel": "HO",
      "medical_specialty": "HO",
      "device_name": "Bed-Patient Activity Monitoring System",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "General Hospital",
      "device_class": "1",
      "definition": "A bed-patient activity monitoring system is intended to monitor activity of patients while lying in a bed using pressure sensors placed on multiple parts of the body or locations under the mattress. The system may indicate by an alarm or other signal when patient activity deviates from assigned pressure prevention parameters.",
      "regulation_number": "880.2400",
      "implant_flag": "N",
      "submission_type_id": "4"
    }
  ]
}