{
  "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": "2026-06-01",
    "results": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "third_party_flag": "N",
      "life_sustain_support_flag": "N",
      "gmp_exempt_flag": "N",
      "summary_malfunction_reporting": "Ineligible",
      "product_code": "OSP",
      "openfda": {
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          "K101801",
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      "review_panel": "OB",
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      "device_name": "Uterine Electromyographic Monitor",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Obstetrics/Gynecology",
      "device_class": "2",
      "definition": "The uterine electromyographic monitor is intended to pick up uterine emg signals from surface electrodes placed on the maternal abdomen.  It produces a uterine activity tracing and monitors women in labor at term gestation with a singleton pregnancy.",
      "regulation_number": "884.2720",
      "implant_flag": "N",
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