Research Catalog

Guidance for industry and FDA staff : expedited review of premarket submissions for devices.

Title
Guidance for industry and FDA staff : expedited review of premarket submissions for devices.
Publication
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]

Available Online

https://purl.fdlp.gov/GPO/LPS111920

Details

Additional Authors
  • Center for Devices and Radiological Health (U.S.)
  • Center for Biologics Evaluation and Research (U.S.)
Description
12 pages : digital, PDF file
Alternative Title
Expedited review of premarket submissions for devices
Subject
Medical instruments and apparatus > United States > Evaluation
Note
  • Title from PDF title page (viewed on Apr. 27, 2009).
  • "February 29, 2008".
System Details (note)
  • Mode of access: Internet at the FDA CBER Web site. Address as of 4/27/09: http://www.fda.gov/cdrh/mdufma/guidance/108.pdf ; current access is available via PURL.
Call Number
GPO Internet HE 20.4802:R 32
OCLC
marcive319439436
Title
Guidance for industry and FDA staff : expedited review of premarket submissions for devices.
Publisher
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]
Type of Content
text
Type of Medium
computer
Type of Carrier
online resource
System Details
Mode of access: Internet at the FDA CBER Web site. Address as of 4/27/09: http://www.fda.gov/cdrh/mdufma/guidance/108.pdf ; current access is available via PURL.
Connect to:
https://purl.fdlp.gov/GPO/LPS111920
Added Author
Center for Devices and Radiological Health (U.S.)
Center for Biologics Evaluation and Research (U.S.)
Gpo Item No.
0499-T-02 (online)
Sudoc No.
HE 20.4802:R 32
View in Legacy Catalog