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        <title>Preventing Superbugs and Protecting Patients Act</title>
        <congress>114</congress>
        <number>4966</number>
        <type>HR</type>
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          <actionDate>2016-04-22</actionDate>
          <text>Referred to the Subcommittee on Health.</text>
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        <title>21st Century Cures Act</title>
        <congress>114</congress>
        <number>34</number>
        <type>HR</type>
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          <actionDate>2016-12-13</actionDate>
          <text>Became Public Law No: 114-255.</text>
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        <text>Placed on Senate Legislative Calendar under General Orders. Calendar No. 417.</text>
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        <text>Committee on Health, Education, Labor, and Pensions. Reported by Senator Alexander with an amendment in the nature of a substitute. Without written report.</text>
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        <text>Committee on Health, Education, Labor, and Pensions. Reported by Senator Alexander with an amendment in the nature of a substitute. Without written report.</text>
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        <text>Committee on Health, Education, Labor, and Pensions. Ordered to be reported with an amendment in the nature of a substitute favorably.</text>
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        <text>Read twice and referred to the Committee on Health, Education, Labor, and Pensions.</text>
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        <fullName>Sen. Murray, Patty [D-WA]</fullName>
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        <lastName>Murray</lastName>
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        <state>WA</state>
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        <pubDate>2016-08-09T20:53:00Z</pubDate>
        <title>S. 2503, Preventing Superbugs and Protecting Patients Act</title>
        <url>https://www.cbo.gov/publication/51888</url>
        <description>As reported by the Senate Committee on Health, Education, Labor, and Pensions on April 5,&amp;nbsp;2016</description>
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        <actionDesc>Introduced in Senate</actionDesc>
        <updateDate>2016-02-19T19:54:59Z</updateDate>
        <text><![CDATA[ <p><b>Preventing Superbugs and Protecting Patients Act</b></p> <p>This bill amends the Federal Food, Drug, and Cosmetic Act to require the Food and Drug Administration (FDA) to identify types of medical devices for which premarket notification must include proposed labeling, including validated instructions regarding cleaning, disinfection, and sterilization.</p> The FDA must issue final guidance regarding when a premarket notification is required for a modification to a medical device.]]></text>
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      <summary>
        <versionCode>01</versionCode>
        <actionDate>2016-04-05</actionDate>
        <actionDesc>Reported to Senate with amendment(s)</actionDesc>
        <updateDate>2016-05-19T18:58:23Z</updateDate>
        <text><![CDATA[ <p><b>Preventing Superbugs and Protecting Patients Act</b></p> <p>(Sec. 2) This bill amends the Federal Food, Drug, and Cosmetic Act to require the Food and Drug Administration (FDA) to identify types of medical devices for which premarket notification must include proposed labeling, including validated instructions regarding cleaning, disinfection, and sterilization.</p> (Sec. 3) The FDA must issue final guidance regarding when a premarket notification is required for a modification to a medical device.]]></text>
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    <title>Preventing Superbugs and Protecting Patients Act</title>
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        <title>Preventing Superbugs and Protecting Patients Act</title>
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        <title>A bill to establish requirements for reusable medical devices relating to cleaning instructions and validation data, and for other purposes.</title>
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        <title>Preventing Superbugs and Protecting Patients Act</title>
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        <title>Preventing Superbugs and Protecting Patients Act</title>
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        <date>2016-04-05T04:00:00Z</date>
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    <latestAction>
      <actionDate>2016-04-05</actionDate>
      <text>Placed on Senate Legislative Calendar under General Orders. Calendar No. 417.</text>
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    <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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