Adverse event reporting for medical devices. 
Running title:  Adverse event reporting for medical devices 

 - 1 online resource (iv, 29 pages) :  illustrations 
<br/><br/> "October 2009."  "OEI-01-08-00110."  CRDP Project record. 
<br/><br/>Includes bibliographical references. 
<br/><br/><label>Subjects--Corporate Names: </label><br/>Center for Devices and Radiological Health (U.S.)
<br/><br/><label>Subjects--Topical Terms: </label><br/>Products liability--Medical instruments and apparatus--Reporting--United States.<br/>Consumer protection--United States.
<br/><br/><label>GPO Item No.: </label>0445-B-07 (online) 
<br/><br/><label>Gov. Doc. Class. No.: </label>HE 1.75:OEI-01-08-00110 
<br/><br/><label>Report. No.: </label>OEI-01-08-00110