{
  "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": "2026-11-02",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "third_party_flag": "Y",
      "life_sustain_support_flag": "N",
      "gmp_exempt_flag": "N",
      "summary_malfunction_reporting": "Eligible",
      "product_code": "NNH",
      "openfda": {},
      "review_panel": "AN",
      "medical_specialty": "AN",
      "device_name": "Needle, Conduction, Anesthesia, Reprocessed",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Anesthesiology",
      "device_class": "2",
      "definition": "A reprocessed needle is a device used to inject local anesthesia into a patient to provide regional anesthesia.  This is the same as \"BSP.\" Reprocessing validation data for this device type must be included in a 510(k) submission. (70 FR 56911, available at https://www.govinfo.gov/content/pkg/FR-2005-09-29/pdf/05-19510.pdf).",
      "regulation_number": "868.5150",
      "implant_flag": "N",
      "submission_type_id": "1"
    }
  ]
}