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(See Related Information)FREQUENTLY USED WEBSITES - February 2003

CDRH Home Page www.fda.gov/cdrh/
Device Advice www.fda.gov/cdrh/devadvice/ ���������
Consumer Information/CDRH www.fda.gov/cdrh/consumer
CDRH Databases www.fda.gov/cdrh/databases.html
510(k) Information & Releasable Database
www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/search.cfm
Product Classification Database
www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpcd/search.cfm
Registration Searchable Database
www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfrl/registra/search.cfm
Listing Searchable Database
www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfrl/Listing/search.cfm
Contacts Listing Database
www.accessdata.fda.gov/scripts/cdrh/cfdocs/contacts/Index.cfm
Premarket Approval Database
www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfPMA/pma.cfm
CDRH Referral List www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfReferral/referral.cfm
Index of CDRH Web Documents� www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfTopic/topicindex/topindx.cfm
Code of Federal Regulations (CFR) www.fda.gov/cdrh/devadvice/365.html
21 CFR www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfcfr/cfrsearch.cfm
DSMICA Staff Directory www.fda.gov/cdrh/dsma/dsmastaf.html
Electronic Products Radiation Control www.fda.gov/cdrh/comp/eprc.html �������������
Export of Medical Devices www.fda.gov/cdrh/devadvice/39.html
Federal Food, Drug, and Cosmetic Act Link to GPO Site
FDA Home Page www.fda.gov/
FDA's Centers Small Business Contacts www.fda.gov/ora/fed_state/Small_Business/sb_guide/centerco.htm
Global Harmonization www.ghtf.org
Good Guidance Practices (GGP) www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfggp/search.cfm
International Program www.fda.gov/cdrh/international/
Medical Device Reporting Home Page www.fda.gov/cdrh/mdr/l
MEDWATCH www.fda.gov/medwatch/index.html
Medical Device Exemptions www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpcd/315.cfm
Medical Device User Fee and Modernization Act of 2002 (MDUFMA) www.fda.gov/cdrh/mdufma
Premarket Approval www.fda.gov/cdrh/devadvice/pma
Premarket Notification (510(k)) www.fda.gov/cdrh/devadvice/314.html
510(k) Paradigm www.fda.gov/cdrh/ode/parad510.html
Establishment Registration and U.S. Agent www.fda.gov/cdrh/devadvice/341.html
Medical Device Listing www.fda.gov/cdrh/devadvice/342.html
Reuse of Single Use Devices www.fda.gov/cdrh/reuse
CDRH Standards Program www.fda.gov/cdrh/stdsprog.html
Third Party Review Program www.fda.gov/cdrh/thirdparty
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Updated 6/11/2003

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