{
  "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": "Y",
      "life_sustain_support_flag": "N",
      "gmp_exempt_flag": "N",
      "summary_malfunction_reporting": "Eligible",
      "product_code": "NKX",
      "openfda": {
        "k_number": [
          "K060648",
          "K050518",
          "K012698",
          "K012579",
          "K030179"
        ],
        "registration_number": [
          "1054713",
          "3032391"
        ],
        "fei_number": [
          "1000114111",
          "3002299608"
        ]
      },
      "review_panel": "OP",
      "medical_specialty": "OP",
      "device_name": "Needle, Phacoemulsification, Reprocessed",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Ophthalmic",
      "device_class": "2",
      "definition": "Needle for phacoemulsification device to remove cataractous lens.  Same as needle for main phacoemulsification device and un-reprocessed needle with product code HQC, except this is a \"reprocessed\" needle.  The Phacoemulsification device is NOT reprocessed, just the needle. 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": "886.4670",
      "implant_flag": "N",
      "submission_type_id": "1"
    }
  ]
}