{
  "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": "2026-04-13",
    "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": "QEH",
      "openfda": {
        "k_number": [
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          "K241385",
          "K201031",
          "K192538",
          "K213800"
        ],
        "registration_number": [
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          "1911916",
          "1920898",
          "1217831",
          "3017509841",
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          "1213809",
          "3005670221",
          "2243072",
          "3013764800",
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      },
      "review_panel": "HO",
      "medical_specialty": "HO",
      "device_name": "Piston Syringe With Neuraxial Connector  Epidural, Peripheral, And/Or Indirect Cerebral Spinal Fluid Contact  ",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "General Hospital",
      "device_class": "2",
      "definition": "A neuraxial piston syringe is intended to inject or withdraw fluid from the neuraxial space with neuraxial specific connections. This product code may include epidural, peripheral, subarachnoid/spinal block, intrathecal and/or intracerebroventricular administration routes. The connector for neuraxial applications is intended to facilitate ANSI/AAMI/ISO 80369-6:2016 compliant neuraxial specific connections.",
      "regulation_number": "880.5860",
      "implant_flag": "N",
      "submission_type_id": "1"
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  ]
}