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.

United States. Food and Drug Administration.

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

Medical instruments and apparatus.

Equipment and Supplies--standards.

Management.

Medical instruments and apparatus--Standards.

Medical Subjects:

United States Food and Drug Administration.

Equipment and Supplies--standards.

United States.

Genre:

Statistics

Statistics.

Physical Description:

iv, 57 pages : digital, PDF file

Other Title:

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]

Notes:

Title from title screen (viewed Feb. 17, 2009).

"January 2009."

Includes bibliographical references.

"GAO-09-190."

Other Format:

United States. Government Acountability Office. Medical devices : FDA should take steps to ensure that high-risk device types are approved through the most stringent premarket review process

OCLC:

310982445