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<bill bill-stage="Introduced-in-Senate" public-private="public">
	<form>
		<distribution-code display="yes">II</distribution-code>
		<congress>111th CONGRESS</congress>
		<session>1st Session</session>
		<legis-num>S. 540</legis-num>
		<current-chamber>IN THE SENATE OF THE UNITED STATES</current-chamber>
		<action>
			<action-date date="20090305">March 5, 2009</action-date>
			<action-desc><sponsor name-id="S055">Mr. Kennedy</sponsor> (for
			 himself, <cosponsor name-id="S057">Mr. Leahy</cosponsor>,
			 <cosponsor name-id="S253">Mr. Durbin</cosponsor>, <cosponsor name-id="S150">Mr.
			 Dodd</cosponsor>, <cosponsor name-id="S172">Mr. Harkin</cosponsor>,
			 <cosponsor name-id="S167">Mr. Bingaman</cosponsor>, <cosponsor name-id="S259">Mr. Reed</cosponsor>, <cosponsor name-id="S313">Mr.
			 Sanders</cosponsor>, <cosponsor name-id="S307">Mr. Brown</cosponsor>,
			 <cosponsor name-id="S309">Mr. Casey</cosponsor>, <cosponsor name-id="S320">Mrs.
			 Hagan</cosponsor>, <cosponsor name-id="S322">Mr. Merkley</cosponsor>,
			 <cosponsor name-id="S316">Mr. Whitehouse</cosponsor>, <cosponsor name-id="S312">Mrs. McCaskill</cosponsor>, <cosponsor name-id="S257">Mr.
			 Johnson</cosponsor>, <cosponsor name-id="S270">Mr. Schumer</cosponsor>,
			 <cosponsor name-id="S326">Mr. Udall of New Mexico</cosponsor>, and
			 <cosponsor name-id="S223">Mrs. Boxer</cosponsor>) introduced the following
			 bill; which was read twice and referred to the
			 <committee-name committee-id="SSHR00">Committee on Health, Education, Labor,
			 and Pensions</committee-name></action-desc>
		</action>
		<legis-type>A BILL</legis-type>
		<official-title>To amend the Federal Food, Drug, and Cosmetic Act with
		  respect to liability under State and local requirements respecting
		  devices.</official-title>
	</form>
	<legis-body>
		<section id="S1" section-type="section-one"><enum>1.</enum><header>Short
			 title</header><text display-inline="no-display-inline">This Act may be cited as
			 the <quote><short-title>Medical Device Safety Act of
			 2009</short-title></quote>.</text>
		</section><section id="idDD53E9E87DA943909477E05AB86C8A07"><enum>2.</enum><header>Liability under
			 state and local requirements respecting devices</header>
			<subsection id="id3972581E594D4A5D86BB5CA32F9C04DB"><enum>(a)</enum><header>Amendment</header><text>Section
			 521 of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 360k) is amended by
			 adding at the end the following:</text>
				<quoted-block display-inline="no-display-inline" id="id7BF62E6D8D234D9C80F065E9F547E819" style="OLC">
					<subsection id="idC2C6C846276C449E8B5D4A9E1D6C8F49"><enum>(c)</enum><header>No effect on
				liability under state law</header><text>Nothing in this section shall be
				construed to modify or otherwise affect any action for damages or the liability
				of any person under the law of any
				State.</text>
					</subsection><after-quoted-block>.</after-quoted-block></quoted-block>
			</subsection><subsection id="id062BCC6745264E6BB9D3B4842A31C634"><enum>(b)</enum><header>Effective date;
			 applicability</header><text>The amendment made by subsection (a) shall—</text>
				<paragraph id="id671FC0B62977437B89DD3399B7169974"><enum>(1)</enum><text>take effect as if
			 included in the enactment of the Medical Device Amendments of 1976 (Public Law
			 94–295); and</text>
				</paragraph><paragraph id="idB7323A969A4C4CCE94076C736FB6EEA4"><enum>(2)</enum><text>apply to any
			 civil action pending or filed on or after the date of enactment of this
			 Act.</text>
				</paragraph></subsection></section></legis-body>
</bill>
