{
  "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": "2026-07-20",
    "results": {
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  "results": [
    {
      "third_party_flag": "N",
      "city": "Northbrook",
      "advisory_committee_description": "Unknown",
      "address_1": "3400 Dundee Rd.",
      "address_2": "",
      "statement_or_summary": "",
      "product_code": "LWM",
      "openfda": {
        "device_name": "Device, Electrical Dental Anesthesia",
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      "applicant": "Pain Prevention Laboratory, Inc.",
      "decision_date": "1987-12-30",
      "decision_code": "SESE",
      "country_code": "US",
      "device_name": "COMFORT MACHINE FOR DESENSITIZATION/ANESTHESIA USE",
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      "contact": "JESS  HALPERN",
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      "k_number": "K873605",
      "state": "IL",
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      "review_advisory_committee": "DE",
      "postal_code": "60062",
      "decision_description": "Substantially Equivalent",
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}