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User fees and refunds for premarket approval applications.

Bibliographic Details
Corporate Authors: Center for Devices and Radiological Health (U.S.), Center for Biologics Evaluation and Research (U.S.)
Format: Government Document eBook
Language:English
Published: Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Devices and Radiological Health : Center for Biologics Evaluation and Research, [2003]
Subjects:
User charges > United States.
Medical instruments and apparatus > Government policy > United States.
Medical instruments and apparatus > Government approval > United States.
Online Access:https://purl.fdlp.gov/GPO/LPS113032
Description
Item Description:Title from PDF title page (viewed on May 22, 2009).
"Document issued on: November 24, 2003".
Electronic resource.
Physical Description:12 pages : digital, PDF file.
Format:Mode of access: Internet at the FDA CBER web site. Address as of 5/22/09: http://www.fda.gov/cdrh/mdufma/guidance/1224.pdf ; current access is available via PURL.