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HHS/FDA RIN: 0910-AG79 Publication ID: Spring 2018 
Title: Electronic Submission of Labeling for Certain Home-Use Devices 

This rule would require medical device establishments listing certain home-use medical devices to submit, in electronic format, the label and package insert of such medical devices listed with FDA. FDA intends to make the information from the submitted labeling accessible by the public through a focused Internet site.

Agency: Department of Health and Human Services(HHS)  Priority: Substantive, Nonsignificant 
RIN Status: Previously published in the Unified Agenda Agenda Stage of Rulemaking: Final Rule Stage 
Major: No  Unfunded Mandates: No 
EO 13771 Designation: Deregulatory 
CFR Citation: 21 CFR 807, subpart F (new)    21 CFR 807.26    21 CFR 807.40    21 CFR 807.3     (To search for a specific CFR, visit the Code of Federal Regulations.)
Legal Authority: sec. 510(j) of the Federal Food, Drug, and Cosmetic Act, 21 U.S.C. 360(j)    sec. 510(p) of the Federal Food, Drug, and Cosmetic Act, 21 U.S.C. 360(p), enacted by the Food and Drug Administration Amendments Act of 2007   
Legal Deadline:  None
Action Date FR Cite
NPRM  10/17/2016  81 FR 71415   
NPRM Comment Period End  01/17/2017 
NPRM; Withdrawal  08/00/2018 
Regulatory Flexibility Analysis Required: No  Government Levels Affected: None 
Federalism: No 
Included in the Regulatory Plan: No 
RIN Data Printed in the FR: No 
Agency Contact:
Madhusoodana Nambiar
Regulatory Counsel
Department of Health and Human Services
Food and Drug Administration
Center for Devices and Radiological Health, WO 66, Room 5518, 10903 New Hampshire Avenue,
Silver Spring, MD 20993
Phone:301 796-5837
Fax:301 847-8145