Real-time premarket approval application (PMA) supplements.

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, [2006]
Subjects:	Medical instruments and apparatus > Evaluation > Government policy > United States.
Online Access:	https://purl.fdlp.gov/GPO/LPS112750

Description
Item Description:	Title from PDF title page (viewed on May 18, 2009). "Document issued on: April 28, 2006". Electronic resource.
Physical Description:	7 pages : digital, PDF file.
Format:	Mode of access: Internet at the FDA CBER web site. Address as of 5/18/09: http://www.fda.gov/cdrh/ode/guidance/673.pdf ; current access is available via PURL.