{
  "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": "Golden",
      "advisory_committee_description": "Cardiovascular",
      "address_1": "6355 Joyce Dr.",
      "address_2": "",
      "statement_or_summary": "",
      "product_code": "JOM",
      "openfda": {
        "registration_number": [
          "2000010846",
          "3012302888",
          "3008514120",
          "9681377",
          "3019130",
          "3010536822",
          "1000589001",
          "3012528160",
          "3008577991",
          "3000126629",
          "3011861727",
          "9610816",
          "2134492",
          "3006146787",
          "3014541700",
          "3020115",
          "2245574",
          "3008717264",
          "3009690509",
          "3009077524",
          "1218950",
          "3016701404",
          "3013783488",
          "3008791915",
          "3007048291"
        ],
        "fei_number": [
          "2000010846",
          "3012302888",
          "3008514120",
          "3019130",
          "3010536822",
          "3002619777",
          "1000589001",
          "3012528160",
          "3008577991",
          "3000126629",
          "3011861727",
          "3006146787",
          "3014541700",
          "3020115",
          "3002807167",
          "2245574",
          "3008717264",
          "3009690509",
          "3009077524",
          "1218950",
          "3016701404",
          "1000300598",
          "3013783488",
          "3008791915",
          "3007048291"
        ],
        "device_name": "Plethysmograph, Photoelectric, Pneumatic Or Hydraulic",
        "medical_specialty_description": "Cardiovascular",
        "regulation_number": "870.2780",
        "device_class": "2"
      },
      "zip_code": "80403",
      "applicant": "Imex Medical Systems, Inc.",
      "decision_date": "1987-06-12",
      "decision_code": "SESE",
      "country_code": "US",
      "device_name": "PULSE CUFF RECORDER MODEL PCR100",
      "advisory_committee": "CV",
      "contact": "ED  BISTRICK",
      "expedited_review_flag": "",
      "k_number": "K863702",
      "state": "CO",
      "date_received": "1986-09-23",
      "review_advisory_committee": "CV",
      "postal_code": "80403",
      "decision_description": "Substantially Equivalent",
      "clearance_type": "Traditional"
    }
  ]
}