United States Government Publishing Office publisher pbl distributor dst United States National Archives and Records Administration Office of the Federal Register author aut Government Organization text government publication eng FR Regulatory Information 2012_register executive 2012-11-24 article Notices D09002ee1c7fc27e3 D09002ee1c7fc28a7 United States Department of Health and Human Services originator org United States Government Agency or Subagency United States Food and Drug Administration originator org United States Government Agency or Subagency The Food and Drug Administration (FDA) is announcing the Web site location where the Agency will post two lists of guidance documents that the Center for Devices and Radiological Health (CDRH) is intending to publish in Fiscal Year (FY) 2013. In addition, FDA has established a docket where stakeholders may provide comments and/or propose draft language for those topics, suggest new or different guidance documents, and comment on the priority of topics for guidance. 77 FR 70449 https://www.govinfo.gov/app/details/FR-2012-11-26/2012-28539 2012-28539 fr26no12-75 4160-01-P Docket No. FDA-2012-N-1021 https://www.govinfo.gov/app/details/FR-2012-11-26/2012-28539 https://www.govinfo.gov/content/pkg/FR-2012-11-26/html/2012-28539.htm https://www.govinfo.gov/content/pkg/FR-2012-11-26/pdf/2012-28539.pdf 2 p. 70449 70450 77 FR 70449 Medical Device User Fee and Modernization Act; Notice to Public of Web Site Location of Fiscal Year 2013 Proposed Guidance Development; Federal Register Vol. 77, Issue NOTICE 2012-28539 DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration Docket No. FDA-2012-N-1021 4160-01-P 2012-28539 Notice.

The Food and Drug Administration (FDA) is announcing the Web site location where the Agency will post two lists of guidance documents that the Center for Devices and Radiological Health (CDRH) is intending to publish in Fiscal Year (FY) 2013. In addition, FDA has established a docket where stakeholders may provide comments and/or propose draft language for those topics, suggest new or different guidance documents, and comment on the priority of topics for guidance.

Submit either electronic or written comments at any time. Philip Desjardins, Center for Devices and Radiological Health, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 66, rm. 5452, Silver Spring, MD 20993-0002, 301- 796-5678. Medical Device User Fee and Modernization Act: Web Site Location of Fiscal Year 2013 Proposed Guidance Development , http://www.fda.gov/MedicalDevices/DeviceRegulationandGuidance/Overview/MDUFAIII/ucm321367.htm http://www.regulations.gov Vol. 77, no. 227 Office of the Federal Register, National Archives and Records Administration 2012-11-26 continuing daily deposited born digital 331 p. Table of Contents: AE 2.7: GS 4.107: AE 2.106: KF70.A2 https://www.govinfo.gov/app/details/FR-2012-11-26 P0b002ee183845b37 0097-6326 0042-1219 0364-1406 769-004-00000-9 000582072 f:fr26no12 https://www.govinfo.gov/app/details/FR-2012-11-26 https://www.govinfo.gov/content/pkg/FR-2012-11-26/pdf/FR-2012-11-26.pdf https://www.govinfo.gov/content/pkg/FR-2012-11-26/xml/FR-2012-11-26.xml fdlp 70355 70676 DGPO 2012-11-24 2024-06-03 FR-2012-11-26 machine generated eng FR FR-2012-11-26 77 227