{
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    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-09-21",
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      "pma_number": "P160048",
      "supplement_number": "S021",
      "applicant": "Senseonics, Incorporated",
      "street_1": "20451 Seneca Meadows Pkwy.",
      "street_2": "",
      "city": "Germantown",
      "state": "MD",
      "zip": "20876",
      "zip_ext": "",
      "generic_name": "Sensor, glucose, implanted, non-adjunctive use",
      "trade_name": "Eversense® E3 Continuous Glucose Monitoring (CGM) System",
      "product_code": "QHJ",
      "advisory_committee": "CH",
      "advisory_committee_description": "Clinical Chemistry",
      "supplement_type": "Panel Track",
      "supplement_reason": "Change Design/Components/Specifications/Material",
      "expedited_review_flag": "N",
      "date_received": "2022-09-30",
      "decision_date": "2023-03-29",
      "docket_number": "23M-1261",
      "fed_reg_notice_date": "2023-04-27",
      "decision_code": "APPR",
      "ao_statement": "Approval for the Eversense® E3 Continuous Glucose Monitoring System for modifying the device to reduce the frequency of calibration.",
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