{
  "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": "2026-11-02",
    "results": {
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  "results": [
    {
      "pma_number": "P080002",
      "supplement_number": "S002",
      "applicant": "Clear Future, Inc.",
      "street_1": "54 W 21st St.",
      "street_2": "Suite 610",
      "city": "New York City",
      "state": "NY",
      "zip": "10010",
      "zip_ext": "",
      "generic_name": "Single-use internal condom",
      "trade_name": "FC2 FEMALE CONDOM",
      "product_code": "MBU",
      "advisory_committee": "OB",
      "advisory_committee_description": "Obstetrics/Gynecology",
      "supplement_type": "Normal 180 Day Track",
      "supplement_reason": "Change Design/Components/Specifications/Material",
      "expedited_review_flag": "N",
      "date_received": "2016-03-01",
      "decision_date": "2017-06-23",
      "docket_number": "",
      "decision_code": "APPR",
      "ao_statement": "Approval for your proposed change in the formulation of the FC2 Female Condom.",
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        "device_name": "Single-Use Internal Condom",
        "medical_specialty_description": "Obstetrics/Gynecology",
        "regulation_number": "884.5340",
        "device_class": "2",
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