{
  "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": "Y",
      "life_sustain_support_flag": "N",
      "gmp_exempt_flag": "N",
      "summary_malfunction_reporting": "Eligible",
      "product_code": "NRW",
      "openfda": {
        "k_number": [
          "K040580"
        ]
      },
      "review_panel": "HO",
      "medical_specialty": "HO",
      "device_name": "Stimulator, Intramuscular, Automatic",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "General Hospital",
      "device_class": "2",
      "definition": "The Automatic Intramuscular Stimulator is a device that aids muscle stimulation by using a method called dry needling for treatment.  The device consists of a main control unit, a hand-held motor unit, and an AC power supply adapter.  The motor unit has a mounted disposal syringe and a needle mounting hardware for a disposable needle, and enables the practitioner to administer treatment with less physical effort.   An EMG needle is used instead of an acupuncture needle because it is less flexible than the acupuncture needle",
      "regulation_number": "880.5580",
      "implant_flag": "N",
      "submission_type_id": "1"
    }
  ]
}