{
  "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": "2026-07-27",
    "results": {
      "skip": 0,
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  "results": [
    {
      "third_party_flag": "N",
      "city": "Waterloo, On",
      "advisory_committee_description": "Cardiovascular",
      "address_1": "180 Frobisher Dr., Unit 1c",
      "address_2": "",
      "statement_or_summary": "Summary",
      "product_code": "PFA",
      "openfda": {
        "registration_number": [
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        "fei_number": [
          "3010521858"
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        "device_name": "Non-Invasive Central Venous Manometer",
        "medical_specialty_description": "Cardiovascular",
        "regulation_number": "870.1140",
        "device_class": "2"
      },
      "zip_code": "N2V 2A2",
      "applicant": "Mespere Lifesciences, Inc.",
      "decision_date": "2013-08-22",
      "decision_code": "SESE",
      "country_code": "CA",
      "device_name": "CENTRAL VENOUS PRESSURE SYSTEM - MESPERE VENUS 1000",
      "advisory_committee": "CV",
      "contact": "HELEN  TAN",
      "expedited_review_flag": "",
      "k_number": "K131085",
      "state": "",
      "date_received": "2013-04-18",
      "review_advisory_committee": "CV",
      "postal_code": "N2V 2A2",
      "decision_description": "Substantially Equivalent",
      "clearance_type": "Traditional"
    }
  ]
}