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Adverse event reporting for medical devices.

Adverse event reporting for medical devices. Running title: Adverse event reporting for medical devices - 1 online resource (iv, 29 pages) : illustrations

"October 2009." "OEI-01-08-00110." CRDP Project record.

Includes bibliographical references.

Subjects--Corporate Names:
Center for Devices and Radiological Health (U.S.)

Subjects--Topical Terms:
Products liability--Medical instruments and apparatus--Reporting--United States.
Consumer protection--United States.

GPO Item No.: 0445-B-07 (online)

Gov. Doc. Class. No.: HE 1.75:OEI-01-08-00110

Report. No.: OEI-01-08-00110

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