October 2019 – Federal Register Recent Federal Regulation Documents

Results 501 - 550 of 2,601
Medical Devices; Orthopedic Devices; Classification of Orthopedic Surgical Instrumentation Designed for Osteochondral Implants With Press-Fit Fixation
Document Number: 2019-23307
Type: Rule
Date: 2019-10-25
Agency: Food and Drug Administration, Department of Health and Human Services
The Food and Drug Administration (FDA or we) is classifying the orthopedic surgical instrumentation designed for osteochondral implants with press-fit fixation into class II (special controls). The special controls that apply to the device type are identified in this order and will be part of the codified language for the orthopedic surgical instrumentation designed for osteochondral implants with press-fit fixation's classification. We are taking this action because we have determined that classifying the device into class II (special controls) will provide a reasonable assurance of safety and effectiveness of the device. We believe this action will also enhance patients' access to beneficial innovative devices, in part by reducing regulatory burdens.
Submission for OMB Review; Comment Request
Document Number: 2019-23306
Type: Notice
Date: 2019-10-25
Agency: Department of Agriculture
Revisions to Safety Standard for Toddler Beds
Document Number: 2019-23305
Type: Rule
Date: 2019-10-25
Agency: Consumer Product Safety Commission, Agencies and Commissions
In February 2017, the U.S. Consumer Product Safety Commission (CPSC) published an update to the consumer product safety standard for toddler beds. The standard incorporated by reference the applicable ASTM voluntary standard. ASTM has since published two revised versions of the voluntary standard for toddler beds. We are publishing this direct final rule revising the CPSC's mandatory standard for toddler beds to incorporate by reference, the most recent version of the applicable ASTM standard.
Medical Devices; Physical Medicine Therapeutic Devices; Classification of the Internal Therapeutic Massager
Document Number: 2019-23304
Type: Rule
Date: 2019-10-25
Agency: Food and Drug Administration, Department of Health and Human Services
The Food and Drug Administration (FDA or we) is classifying the internal therapeutic massager into class II (special controls). The special controls that apply to the device type are identified in this order and will be part of the codified language for the internal therapeutic massager's classification. We are taking this action because we have determined that classifying the device into class II (special controls) will provide a reasonable assurance of safety and effectiveness of the device. We believe this action will also enhance patients' access to beneficial innovative devices, in part by reducing regulatory burdens.
Submission for OMB Review; Comment Request
Document Number: 2019-23303
Type: Notice
Date: 2019-10-25
Agency: Department of Agriculture
Petition for Waiver of Compliance
Document Number: 2019-23302
Type: Notice
Date: 2019-10-25
Agency: Federal Railroad Administration, Department of Transportation
Petition for Waiver of Compliance
Document Number: 2019-23301
Type: Notice
Date: 2019-10-25
Agency: Federal Railroad Administration, Department of Transportation
Submission for OMB Review; Provision of Services in Intergovernmental IV-D; Federally Approved Forms
Document Number: 2019-23300
Type: Notice
Date: 2019-10-25
Agency: Department of Health and Human Services, Administration for Children and Families
This is a revision to an existing data collection which expires December 31, 2019. This data collection consists of 13 intergovernmental forms used by States and other entities to process intergovernmental child support cases. This request is for minor revisions to the approved forms.
Agency Information Collection Activities; Submission for OMB Review; Comment Request; Operations Mining Under a Body of Water
Document Number: 2019-23299
Type: Notice
Date: 2019-10-25
Agency: Department of Labor, Office of the Secretary
The Department of Labor (DOL) is submitting the Mine Safety and Health Administration (MSHA) sponsored information collection request (ICR) titled, ``Operations Mining Under a Body of Water,'' to the Office of Management and Budget (OMB) for review and approval for continued use, without change, in accordance with the Paperwork Reduction Act of 1995 (PRA). Public comments on the ICR are invited.
Agency Information Collection Activities; Submission for OMB Review; Comment Request; Post Enrollment Data Collection for Job Corps Participants
Document Number: 2019-23298
Type: Notice
Date: 2019-10-25
Agency: Department of Labor, Office of the Secretary
The Department of Labor (DOL) is submitting the Employment Training Administration (ETA) sponsored information collection request (ICR) revision titled, ``Post Enrollment Data Collection for Job Corps Participants,'' to the Office of Management and Budget (OMB) for review and approval for use in accordance with the Paperwork Reduction Act (PRA) of 1995. Public comments on the ICR are invited.
Agency Information Collection Activities: Announcement of the Office of Management and Budget (OMB) Control Numbers Under the Paperwork Reduction Act
Document Number: 2019-23297
Type: Notice
Date: 2019-10-25
Agency: Department of Labor, Occupational Safety and Health Administration
The Occupational Safety and Health Administration announces that OMB extended approval for information collection requirements found in OSHA's standards and regulations outlined in this notice. OSHA sought approval of these requirements under the Paperwork Reduction Act of 1995 (PRA), and, as required by that Act, is announcing the approval numbers and expiration dates for these requirements and regulations.
Hexavalent Chromium Standards; Extension of the Office of Management and Budget's (OMB) Approval of Information Collection (Paperwork) Requirements
Document Number: 2019-23296
Type: Notice
Date: 2019-10-25
Agency: Department of Labor, Occupational Safety and Health Administration
OSHA solicits public comments concerning the proposal to extend OMB approval of the information collection requirements specified in the Hexavalent Chromium standards for General Industry, Shipyard Employment, and Construction.
Agency Information Collection Activities: Announcement of the Office of Management and Budget (OMB) Control Numbers Under the Paperwork Reduction Act
Document Number: 2019-23295
Type: Notice
Date: 2019-10-25
Agency: Department of Labor, Occupational Safety and Health Administration
Comporting with Executive Order 13563, ``Improving Regulations and Regulatory Review,'' and consistent with Executive Order 13777, ``Enforcing the Regulatory Reform Agenda,'' OSHA removed or revised outdated, duplicative, unnecessary, and inconsistent requirements in safety and health standards. Standards Improvement ProjectPhase IV (SIP-IV) was published May 14, 2019 (84 FR 21416, Docket Number OSHA- 2012-0007). This final rule reduces regulatory burden while maintaining or enhancing worker safety and health, and improving privacy protections. The Occupational Safety and Health Administration announces an OMB extension of approval for a number of information collection requirements found in the final rule. OSHA sought approval of these requirements under the Paperwork Reduction Act of 1995 (PRA), and, as required by that Act, is announcing the approval numbers and expiration dates for these requirements.
Procurement List; Deletions
Document Number: 2019-23294
Type: Notice
Date: 2019-10-25
Agency: Committee for Purchase From People Who Are Blind or Severely Disabled, Agencies and Commissions
This action deletes a product and services from the Procurement List that were furnished by nonprofit agencies employing persons who are blind or have other severe disabilities.
Procurement List; Proposed Additions
Document Number: 2019-23293
Type: Notice
Date: 2019-10-25
Agency: Committee for Purchase From People Who Are Blind or Severely Disabled, Agencies and Commissions
The Committee is proposing to add products to the Procurement List that will be furnished by nonprofit agencies employing persons who are blind or have other severe disabilities.
National Institute on Drug Abuse; Notice of Closed Meetings
Document Number: 2019-23291
Type: Notice
Date: 2019-10-25
Agency: Department of Health and Human Services, National Institutes of Health
National Institute on Aging; Notice of Closed Meeting
Document Number: 2019-23290
Type: Notice
Date: 2019-10-25
Agency: Department of Health and Human Services, National Institutes of Health
National Institute on Aging; Notice of Closed Meeting
Document Number: 2019-23289
Type: Notice
Date: 2019-10-25
Agency: Department of Health and Human Services, National Institutes of Health
National Institute on Aging; Notice of Closed Meeting
Document Number: 2019-23288
Type: Notice
Date: 2019-10-25
Agency: Department of Health and Human Services, National Institutes of Health
National Cancer Institute; Amended Notice of Meeting
Document Number: 2019-23287
Type: Notice
Date: 2019-10-25
Agency: Department of Health and Human Services, National Institutes of Health
Center for Scientific Review; Notice of Closed Meetings
Document Number: 2019-23286
Type: Notice
Date: 2019-10-25
Agency: Department of Health and Human Services, National Institutes of Health
Center for Scientific Review; Amended Notice of Meeting
Document Number: 2019-23285
Type: Notice
Date: 2019-10-25
Agency: Department of Health and Human Services, National Institutes of Health
Airworthiness Directives; Airbus SAS Airplanes
Document Number: 2019-23284
Type: Rule
Date: 2019-10-25
Agency: Federal Aviation Administration, Department of Transportation
The FAA is adopting a new airworthiness directive (AD) for all Airbus SAS Model A330-200, -200F, and -300 series airplanes. This AD was prompted by a determination that new or more restrictive airworthiness limitations are necessary. This AD requires revising the existing maintenance or inspection program, as applicable, to incorporate new or more restrictive airworthiness limitations. The FAA is issuing this AD to address the unsafe condition on these products.
Submission for OMB Review; 30-Day Comment Request; Summer Research Internship Program (National Institute on Drug Abuse)
Document Number: 2019-23283
Type: Notice
Date: 2019-10-25
Agency: Department of Health and Human Services, National Institutes of Health
In compliance with the Paperwork Reduction Act of 1995, the National Institutes of Health (NIH) has submitted to the Office of Management and Budget (OMB) a request for review and approval of the information collection listed below.
National Cancer Institute; Amended Notice of Meeting
Document Number: 2019-23282
Type: Notice
Date: 2019-10-25
Agency: Department of Health and Human Services, National Institutes of Health
National Institute of Allergy and Infectious Diseases; Notice of Closed Meeting
Document Number: 2019-23281
Type: Notice
Date: 2019-10-25
Agency: Department of Health and Human Services, National Institutes of Health
National Center for Advancing Translational Sciences; Notice of Workshop
Document Number: 2019-23280
Type: Notice
Date: 2019-10-25
Agency: Department of Health and Human Services, National Institutes of Health
National Institute on Aging; Notice of Closed Meeting
Document Number: 2019-23279
Type: Notice
Date: 2019-10-25
Agency: Department of Health and Human Services, National Institutes of Health
Center for Scientific Review; Notice of Closed Meetings
Document Number: 2019-23278
Type: Notice
Date: 2019-10-25
Agency: Department of Health and Human Services, National Institutes of Health
Notice of Public Meeting of the Florida Advisory Committee
Document Number: 2019-23275
Type: Notice
Date: 2019-10-25
Agency: Commission on Civil Rights
Notice is hereby given, pursuant to the provisions of the rules and regulations of the U.S. Commission on Civil Rights (Commission) and the Federal Advisory Committee Act that the Florida Advisory Committee (Committee) will hold a meeting on Thursday, October 31, 2019, at 3:00 p.m. (EST). for the purpose of reviewing received testimony and discussing next steps in hearing testimony regarding Voters Suppression and Disenfranchisement Issues.
Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Administrative Procedures for Clinical Laboratory Improvement Amendments Categorization
Document Number: 2019-23274
Type: Notice
Date: 2019-10-25
Agency: Food and Drug Administration, Department of Health and Human Services
The Food and Drug Administration (FDA or we) is announcing that a proposed collection of information has been submitted to the Office of Management and Budget (OMB) for review and clearance under the Paperwork Reduction Act of 1995.
Agency Information Collection Activities; Proposed Collection; Comment Request; Planning for the Effects of High Absenteeism To Ensure Availability of Medically Necessary Drug Products
Document Number: 2019-23272
Type: Notice
Date: 2019-10-25
Agency: Food and Drug Administration, Department of Health and Human Services
The Food and Drug Administration (FDA or Agency) is announcing an opportunity for public comment on the proposed collection of certain information by the Agency. Under the Paperwork Reduction Act of 1995 (PRA), Federal Agencies are required to publish notice in the Federal Register concerning each proposed collection of information, including each proposed extension of an existing collection of information, and to allow 60 days for public comment in response to the notice. This notice solicits comments on the information collection for the guidance on planning for the effects of high absenteeism to ensure availability of medically necessary drug products.
Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Data To Support Social and Behavioral Research as Used by the Food and Drug Administration
Document Number: 2019-23268
Type: Notice
Date: 2019-10-25
Agency: Food and Drug Administration, Department of Health and Human Services
The Food and Drug Administration (FDA) is announcing that a proposed collection of information has been submitted to the Office of Management and Budget (OMB) for review and clearance under the Paperwork Reduction Act of 1995.
Fisheries of the Caribbean, Gulf of Mexico, and South Atlantic; Snapper-Grouper Fishery of the South Atlantic Region; Regulatory Amendment 26
Document Number: 2019-23267
Type: Proposed Rule
Date: 2019-10-25
Agency: Department of Commerce, National Oceanic and Atmospheric Administration
NMFS proposes to implement recreational sector management measures described in Vision Blueprint Recreational Regulatory Amendment 26 (Regulatory Amendment 26) to the Fishery Management Plan for the Snapper-Grouper Fishery of the South Atlantic Region (Snapper- Grouper FMP), as prepared and submitted by the South Atlantic Fishery Management Council (Council). For the recreational sector, this proposed rule would remove the minimum size limits for queen snapper, silk snapper, and blackfin snapper, reduce the minimum size limit for gray triggerfish in the exclusive economic zone (EEZ) off the east coast of Florida, and modify the 20-fish snapper-grouper aggregate bag limit. The purpose of this proposed rule is to minimize regulatory discards to the extent practicable, improve regulatory compliance among fishers, and increase consistency among regulations.
Submission for OMB Review; Comment Request
Document Number: 2019-23266
Type: Notice
Date: 2019-10-25
Agency: Department of Defense, Office of the Secretary
The Department of Defense has submitted to OMB for clearance the following proposal for collection of information under the provisions of the Paperwork Reduction Act.
Pediatric Stakeholder Meeting; Public Meeting; Request for Comments
Document Number: 2019-23264
Type: Notice
Date: 2019-10-25
Agency: Food and Drug Administration, Department of Health and Human Services
The Food and Drug Administration's (FDA or the Agency) Office of Pediatric Therapeutics (OPT), the Center for Drug Evaluation and Research (CDER) and the Center for Biologics Evaluation and Research (CBER) are announcing a public meeting seeking input from patient/ parent groups, consumer groups, regulated industry, academia, and other interested parties to obtain any recommendations or information relevant to the report to Congress that FDA is required to submit concerning pediatrics, as outlined in section 508 of the Food and Drug Administration Safety and Innovation Act (FDASIA) (see the SUPPLEMENTARY INFORMATION section for additional background information).
Sunday Riley Modern Skincare, LLC; Analysis To Aid Public Comment
Document Number: 2019-23263
Type: Notice
Date: 2019-10-25
Agency: Federal Trade Commission, Agencies and Commissions
The consent agreement in this matter settles alleged violations of federal law prohibiting unfair or deceptive acts or practices. The attached Analysis to Aid Public Comment describes both the allegations in the complaint and the terms of the consent order embodied in the consent agreementthat would settle these allegations.