Skip to : [Content] [Navigation]
 
FDA Federal Register Notices - Archives

2008 | 2007 | 2006 | 2005 | 2004 | 2003 | 2002 | 2001

FDA Federal Register Notices - 2009 Releases
Federal Register: Hematology and Pathology Devices Panel of the Medical Devices Advisory Committee; Notice of Meeting
 June 9, 2009
Federal Register: Draft Guidance for Industry on Presenting Risk Information in Prescription Drug and Medical Device Promotion; Availability
 May 27, 2009
Federal Register: Temporary Deferment of Activities Relating to Medical Device Submissions
 May 21, 2009
Federal Register: Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Electronic Data Collection Using MedWatch\Plus\ Portal and Rational Questionnaire
 May 20, 2009
Federal Register: Gastroenterology and Urology Devices Panel of the Medical Devices Advisory Committee; Notice of Meeting
 May 20, 2009
Federal Register: Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Medical Device Reporting: Manufacturer, Importer, User Facility, and Distributor Reporting
 May 19, 2009
Federal Register: Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Emergency Shortages Data Collection System (formerly "Emergency Medical Device Shortages Program Survey")
 May 8, 2009
Federal Register: Implementation of Post-Approval Studies for Medical Devices; Public Workshop
 May 6, 2009
Federal Register: Pediatric Device Consortia Grant Program
 May 4, 2009
Federal Register: Anesthesiology and Respiratory Therapy Devices Panel of the Medical Devices Advisory Committee; Notice of Meeting
 April 28, 2009
Federal Register: Neurological Devices Panel of the Medical Devices Advisory Committee; Notice of Meeting
 April 28, 2009
Federal Register: Computational Modeling for Cardiovascular Devices; Public Workshop
 April 27, 2009
Federal Register: Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Financial Disclosure by Clinical Investigators
 April 22, 2009
Federal Register: Draft Guidance for Industry and Food and Drug Administration Staff: Investigational Device Exemption Guidance for Retinal Prostheses
 April 17, 2009
Federal Register: Medical Devices; Order for Certain Class III Devices; Submission of Safety and Effectiveness Information
 April 9, 2009
Federal Register: Circulatory System Devices Panel of the Medical Devices Advisory Committee; Notice of Meeting
 April 7, 2009
Federal Register: Medical Devices; Technical Amendment
 April 1, 2009
Federal Register: Medical Devices; Availability of Safety and Effectiveness Summaries for Premarket Approval Applications
 March 19, 2009
Federal Register: Food and Drug Administration Modernization Act of 1997: Modifications to the List of Recognized Standards, Recognition List Number: 021
 March 18, 2009
Federal Register: Draft Guidance for Industry and Food and Drug Administration; User Fees and Refunds for Premarket Approval Applications; Availability
 March 16, 2009
Federal Register: Ophthalmic Devices Panel of the Medical Devices Advisory Committee; Notice of Meeting
 March 12, 2009
Federal Register: Agency Information Collection Activities; Submission for OMB Review; Comment Request; Guidance for Clinical Trial Sponsors: Establishment and Operation of Clinical Trial Data Monitoring Committees
 March 10, 2009
Federal Register: Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Reclassification Petitions for Medical Devices
 March 9, 2009
Federal Register: Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Medical Device Recall Authority
 February 26, 2009
Federal Register: Agency Information Collection Activities; Proposed Collection; Comment Request; Medical Device Reporting: Manufacturer, Importer, User Facility, and Distributor Reporting
 February 25, 2009
Federal Register: Circulatory System Devices Panel of the Medical Devices Advisory Committee Meeting on March 18, 2009
February 19, 2009
Federal Register: Agency Information Collection Activities; Submission for OMB Review; Comment Request; Guidance for Industry and FDA Staff; Compliance With the MDUFMA Act of 2002, as Amended: Prominent and Conspicuous Mark of Manufacturers on Single-Use Devices
 February 11, 2009
Federal Register: Medical Devices; Availability of Safety and Effectiveness Summaries for Premarket Approval Applications
 February 10, 2009
Federal Register: Agency Information Collection Activities; Announcement of OMB Approval; Guidance for Industry and Food and Drug Administration Staff; "Class II Special Controls Guidance Document: Labeling for Natural Rubber Latex Condoms Class CFR 884.5300"
 January 28, 2009
Federal Register: Institutional Review Boards; Registration Requirements
 January 15, 2009
Federal Register: Unique Device Identification System; Public Workshop; Request for Comments
January 15, 2009
Federal Register: Advisory Committees; Tentative Schedule of Meetings for 2009
 January 13, 2009
Federal Register: Guidance for Industry: Good Reprint Practices for the Distribution of Medical Journal Articles and Medical or Scientific Reference Publications on Unapproved New Uses of Approved Drugs and Approved or Cleared Medical Devices; Availability
 January 13, 2009
Federal Register: Draft Guidance for Industry and Food and Drug Administration Staff; Assay Migration Studies for In Vitro Diagnostic Devices; Availability
 January 6, 2009
Federal Register: Guidance for Industry and Food and Drug Administration Staff; Class II Special Controls Guidance Document: Nucleic Acid Amplification Assay for the Detection of Enterovirus RNA; Availability
 January 2, 2009
Federal Register: Medical Devices; Immunology and Microbiology Devices; Classification of Enterovirus Nucleic Acid Assay
 January 2, 2009
  Back to Top
 
 

More CDRH Releases

Federal Register Notices
Guidance Documents

CDRH Resources

Current FDA Warning Letter Database
Archived FDA Warning Letter Database
Releasable 510(k)s
Releasable PMAs
Releasable Establishment Registrations
Releasable Device Listings
Good Guidance Practices
More CDRH databases

More FDA Articles

Medical Device & Diagnostic Industry
In Vitro Diagnostic Technology
Pharmaceutical & Medical Packaging News