Guidance for industry and FDA staff : interactive review for medical device submissions, 510(k)s, original PMAs, PMA supplements, original BLAs, and BLA 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, [2008]
Subjects:	Medical instruments and apparatus > United States > Evaluation. User charges > United States.
Online Access:	https://purl.fdlp.gov/GPO/LPS111915

Description
Item Description:	Title from PDF title page (viewed on April 27, 2008). "February 28, 2008". Electronic resource.
Physical Description:	11 pages : digital, PDF file.
Format:	Mode of access: Internet at the FDA CBER Web site. Address as of 4/27/09: http://www.fda.gov/cdrh/ode/guidance/1655.pdf ; current access is available via PURL.