{
  "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,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "third_party_flag": "N",
      "life_sustain_support_flag": "N",
      "gmp_exempt_flag": "N",
      "summary_malfunction_reporting": "Ineligible",
      "product_code": "PRJ",
      "openfda": {
        "k_number": [
          "K161521",
          "K190225"
        ],
        "registration_number": [
          "1058584",
          "2219920"
        ],
        "fei_number": [
          "1000219637",
          "2219920"
        ]
      },
      "review_panel": "CH",
      "medical_specialty": "CH",
      "device_name": "Capillary Blood Collection Device For Alternative Site Collection",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Clinical Chemistry",
      "device_class": "2",
      "definition": "A capillary blood collection device with or without integrated micro-needles is a blood collection device intended to collect and/or transport capillary whole blood specimens for testing of clinical analytes.",
      "regulation_number": "862.1675",
      "implant_flag": "N",
      "submission_type_id": "1"
    }
  ]
}