Medical devices : are current regulations doing enough for patients? : hearing before the Subcommittee on Health of the Committee on Energy and Commerce, House of Representatives, One Hundred Eleventh Congress, first session, June 18, 2009.

Format:

Book

Government document

Author/Creator:

United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health

Language:

English

Subjects (All):

Medical instruments and apparatus--Safety regulations--United States.

Medical instruments and apparatus.

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

Medical instruments and apparatus--Safety regulations.

Medical instruments and apparatus--Standards.

United States.

Genre:

Legislative hearings

Legislative hearings.

Physical Description:

1 online resource (v, 99 pages) : illustrations

Place of Publication:

Washington : U.S. G.P.O., 2012.

Contents:

Medical devices: shortcomings in FDA's premarket review, postmarket surveillance, and inspections of device manufacturing establishments.

Notes:

Title from title screen (viewed on Sept. 13, 2012).

Paper version available for sale by the Supt. of Docs., U.S.G.P.O.

Includes bibliographical references.

"Serial no. 111-52."

Other Format:

Print version: United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health. Medical devices

Microfiche: United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health. Medical devices

OCLC:

809854158