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    <updateDate>2023-01-11T13:36:29Z</updateDate>
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    <originChamber>Senate</originChamber>
    <type>S</type>
    <introducedDate>2017-05-08</introducedDate>
    <congress>115</congress>
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        <systemCode>sshr00</systemCode>
        <name>Health, Education, Labor, and Pensions Committee</name>
        <chamber>Senate</chamber>
        <type>Standing</type>
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          <item>
            <name>Referred to</name>
            <date>2017-05-08T23:22:41Z</date>
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      <item>
        <title>FDA Reauthorization Act of 2017</title>
        <congress>115</congress>
        <number>934</number>
        <type>S</type>
        <latestAction>
          <actionDate>2017-05-11</actionDate>
          <text>Placed on Senate Legislative Calendar under General Orders. Calendar No. 76.</text>
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            <type>Related bill</type>
            <identifiedBy>CRS</identifiedBy>
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      <item>
        <title>Risk-Based Classification of Accessories Act of 2017</title>
        <congress>115</congress>
        <number>2144</number>
        <type>HR</type>
        <latestAction>
          <actionDate>2017-04-28</actionDate>
          <text>Referred to the Subcommittee on Health.</text>
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            <identifiedBy>CRS</identifiedBy>
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        <actionDate>2017-05-08</actionDate>
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            <systemCode>sshr00</systemCode>
            <name>Health, Education, Labor, and Pensions Committee</name>
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        <sourceSystem>
          <name>Senate</name>
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        <text>Read twice and referred to the Committee on Health, Education, Labor, and Pensions.</text>
        <type>IntroReferral</type>
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      <item>
        <actionDate>2017-05-08</actionDate>
        <text>Introduced in Senate</text>
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          <name>Library of Congress</name>
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    <sponsors>
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        <bioguideId>R000307</bioguideId>
        <fullName>Sen. Roberts, Pat [R-KS]</fullName>
        <firstName>PAT</firstName>
        <lastName>ROBERTS</lastName>
        <party>R</party>
        <state>KS</state>
        <isByRequest>N</isByRequest>
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    <cosponsors>
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        <bioguideId>D000607</bioguideId>
        <fullName>Sen. Donnelly, Joe [D-IN]</fullName>
        <firstName>Joe</firstName>
        <lastName>Donnelly</lastName>
        <party>D</party>
        <state>IN</state>
        <sponsorshipDate>2017-05-08</sponsorshipDate>
        <isOriginalCosponsor>True</isOriginalCosponsor>
      </item>
      <item>
        <bioguideId>B001135</bioguideId>
        <fullName>Sen. Burr, Richard [R-NC]</fullName>
        <firstName>Richard</firstName>
        <lastName>Burr</lastName>
        <party>R</party>
        <state>NC</state>
        <middleName>Mauze</middleName>
        <sponsorshipDate>2017-05-08</sponsorshipDate>
        <isOriginalCosponsor>True</isOriginalCosponsor>
      </item>
    </cosponsors>
    <policyArea>
      <name>Health</name>
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    <subjects>
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        <item>
          <name>Drug safety, medical device, and laboratory regulation</name>
        </item>
        <item>
          <name>Government information and archives</name>
        </item>
        <item>
          <name>Health technology, devices, supplies</name>
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      </legislativeSubjects>
      <policyArea>
        <name>Health</name>
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    <summaries>
      <summary>
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        <actionDate>2017-05-08</actionDate>
        <actionDesc>Introduced in Senate</actionDesc>
        <updateDate>2019-04-17T18:56:44Z</updateDate>
        <text><![CDATA[ <p><b>Risk-Based Classification of Accessories Act of 2017</b></p> <p>This bill revises how accessories to medical devices are classified. Specifically, the Food and Drug Administration must classify accessories based on the risks when used as intended<b>,</b> notwithstanding the classification of any other device with which such accessory is intended to be used. </p>]]></text>
      </summary>
    </summaries>
    <title>Realizing Intended Safety for Certain Accessories Act of 2017</title>
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        <titleType>Display Title</titleType>
        <title>Realizing Intended Safety for Certain Accessories Act of 2017</title>
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        <titleType>Official Title as Introduced</titleType>
        <title>A bill to amend the Federal Food, Drug, and Cosmetic Act to provide for the appropriate, risk-based classification of device accessories based on intended use.</title>
        <billTextVersionName>Introduced in Senate</billTextVersionName>
        <billTextVersionCode>IS</billTextVersionCode>
      </item>
      <item>
        <titleType>Short Titles as Introduced</titleType>
        <title>Realizing Intended Safety for Certain Accessories Act of 2017</title>
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        <type>Introduced in Senate</type>
        <date>2017-05-08T04:00:00Z</date>
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    <latestAction>
      <actionDate>2017-05-08</actionDate>
      <text>Read twice and referred to the Committee on Health, Education, Labor, and Pensions.</text>
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    <dc:language>EN</dc:language>
    <dc:rights>Pursuant to Title 17 Section 105 of the United States Code, this file is not subject to copyright protection and is in the public domain.</dc:rights>
    <dc:contributor>Congressional Research Service, Library of Congress</dc:contributor>
    <dc:description>This file contains bill summaries and statuses for federal legislation. A bill summary describes the most significant provisions of a piece of legislation and details the effects the legislative text may have on current law and federal programs. Bill summaries are authored by the Congressional Research Service (CRS) of the Library of Congress. As stated in Public Law 91-510 (2 USC 166 (d)(6)), one of the duties of CRS is "to prepare summaries and digests of bills and resolutions of a public general nature introduced in the Senate or House of Representatives". For more information, refer to the User Guide that accompanies this file.</dc:description>
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