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2014-10-07
article
Medical Devices; Technical Amendment
Rules and Regulations
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D09002ee1bdc3d110
United States
Department of Health and Human Services
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United States Government Agency or Subagency
United States
Food and Drug Administration
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United States Government Agency or Subagency
The Food and Drug Administration (FDA) is amending certain medical device regulations to correct minor errors in the Code of Federal Regulations (CFR). This action is editorial in nature and is intended to correct outdated Web site addresses.
79 FR 50551
https://www.govinfo.gov/app/details/FR-2014-08-25/2014-20107
2014-20107
fr25au14-5
4164-01-P
Docket No. FDA-2014-N-0011
https://www.govinfo.gov/app/details/FR-2014-08-25/2014-20107
https://www.govinfo.gov/content/pkg/FR-2014-08-25/html/2014-20107.htm
https://www.govinfo.gov/content/pkg/FR-2014-08-25/pdf/2014-20107.pdf
Medical Devices
Blood
Packaging and Containers
Biologics
Laboratories
2 p.
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79 FR 50551
Code of Federal Regulations
Title 21 Part 862
21 CFR Part 862
Code of Federal Regulations
Title 21 Part 864
21 CFR Part 864
Code of Federal Regulations
Title 21 Part 866
21 CFR Part 866
Code of Federal Regulations
Title 21 Part 872
21 CFR Part 872
Medical Devices; Technical Amendment; Federal Register Vol. 79, Issue
RULE
2014-20107
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
2014-08-25
Docket No. FDA-2014-N-0011
4164-01-P
2014-20107
Final rule; technical amendment.
The Food and Drug Administration (FDA) is amending certain medical device regulations to correct minor errors in the Code of Federal Regulations (CFR). This action is editorial in nature and is intended to correct outdated Web site addresses.
This rule is effective August 25, 2014.
Aaron Josephson, Center for Devices and Radiological Health, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 66, Rm. 5449, Silver Spring, MD 20993-0002, 301- 796-5178.
Medical Devices
Blood
Packaging and Containers
Biologics
Laboratories
Medical Devices
,
http://www.fda.gov/AboutFDA/CentersOffices/OfficeofMedicalProductsandTobacco/CDRH/CDRHOmbudsman/default.htm
http://www.fda.gov/cdrh.guidance.html
http://www.fda.gov/MedicalDevices/DeviceRegulationandGuidance/GuidanceDocuments/default.htm
Federal Register
Vol. 79, no. 164
Office of the Federal Register, National Archives and Records Administration
2014-08-25
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309 p.
Table of Contents:
AE 2.7:
GS 4.107:
AE 2.106:
KF70.A2
https://www.govinfo.gov/app/details/FR-2014-08-25
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0097-6326
0042-1219
0364-1406
769-004-00000-9
000582072
f:fr25au14
https://www.govinfo.gov/app/details/FR-2014-08-25
https://www.govinfo.gov/content/pkg/FR-2014-08-25/pdf/FR-2014-08-25.pdf
https://www.govinfo.gov/content/pkg/FR-2014-08-25/xml/FR-2014-08-25.xml
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