Medical devices : FDA should take steps to ensure that high-risk device types are approved through the most stringent premarket review process : report to congressional addressees.

Format:

Book

Government document

Author/Creator:

United States. Government Accountability Office.

Language:

English

Subjects (All):

United States. Food and Drug Administration--Management.

United States.

United States. Food and Drug Administration.

Medical instruments and apparatus--Standards--United States.

Medical instruments and apparatus.

Medical instruments and apparatus--Standards.

Management.

Physical Description:

1 online resource (iv, 57 pages, digital, PDF file)

Other Title:

Medical devices : Food and Drug Administration should take steps to ensure that high risk device types are approved through the most stringent premarket review process

Food and Drug Administration should take steps to ensure that high-risk device types are approved through the most stringent premarket review process

Medical device premarket review

Place of Publication:

[Washington, D.C.] : U.S. Govt. Accountability Office, [2009]

System Details:

text file

Notes:

Record is based on bibliographic data in ProQuest U.S. Congressional Research Digital Collection. Reuse except for individual research requires license from ProQuest, LLC.

Includes bibliographical references.

Electronic reproduction. [Bethesda, Md.] : ProQuest, 2004. digital, PDF file. ProQuest U.S. Congressional Research Digital Collection. Mode of access: World Wide Web via ProQuest website.

Other Format:

Print version: United States. Government Accountability Office. Medical devices

Microfiche version: United States. Government Accountability Office. Medical devices. CIS 2009 J942-59

Access Restriction:

Restricted for use by site license.