21 U.S. Code § 360c–1 - Reporting

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The Secretary of Health and Human Services shall annually post on the Internet Web site of the Food and Drug Administration—
(1) the number and type of class I and class II devices reclassified as class II or class III in the previous calendar year under section 360c (e)(1) of this title;
(2) the number and type of class II and class III devices reclassified as class I or class II in the previous calendar year under such section 360c (e)(1) of this title; and
(3) the number and type of devices reclassified in the previous calendar year under section 360e of this title.

Source

(Pub. L. 112–144, title VI, § 608(c),July 9, 2012, 126 Stat. 1059.)
Codification

Section was enacted as part of the Food and Drug Administration Safety and Innovation Act, and not as part of the Federal Food, Drug, and Cosmetic Act which comprises this chapter.

This is a list of parts within the Code of Federal Regulations for which this US Code section provides rulemaking authority.

This list is taken from the Parallel Table of Authorities and Rules provided by GPO [Government Printing Office].

It is not guaranteed to be accurate or up-to-date, though we do refresh the database weekly. More limitations on accuracy are described at the GPO site.


21 CFR - Food and Drugs

21 CFR Part 3 - PRODUCT JURISDICTION

21 CFR Part 4 - REGULATION OF COMBINATION PRODUCTS

21 CFR Part 5 - ORGANIZATION

21 CFR Part 7 - ENFORCEMENT POLICY

21 CFR Part 10 - ADMINISTRATIVE PRACTICES AND PROCEDURES

21 CFR Part 11 - ELECTRONIC RECORDS; ELECTRONIC SIGNATURES

21 CFR Part 12 - FORMAL EVIDENTIARY PUBLIC HEARING

21 CFR Part 13 - PUBLIC HEARING BEFORE A PUBLIC BOARD OF INQUIRY

21 CFR Part 14 - PUBLIC HEARING BEFORE A PUBLIC ADVISORY COMMITTEE

21 CFR Part 15 - PUBLIC HEARING BEFORE THE COMMISSIONER

21 CFR Part 16 - REGULATORY HEARING BEFORE THE FOOD AND DRUG ADMINISTRATION

21 CFR Part 17 - CIVIL MONEY PENALTIES HEARINGS

21 CFR Part 20 - PUBLIC INFORMATION

21 CFR Part 25 - ENVIRONMENTAL IMPACT CONSIDERATIONS

21 CFR Part 26 - MUTUAL RECOGNITION OF PHARMACEUTICAL GOOD MANUFACTURING PRACTICE REPORTS, MEDICAL DEVICE QUALITY SYSTEM AUDIT REPORTS, AND CERTAIN MEDICAL DEVICE PRODUCT EVALUATION REPORTS: UNITED STATES AND THE EUROPEAN COMMUNITY

21 CFR Part 50 - PROTECTION OF HUMAN SUBJECTS

21 CFR Part 54 - FINANCIAL DISCLOSURE BY CLINICAL INVESTIGATORS

21 CFR Part 56 - INSTITUTIONAL REVIEW BOARDS

21 CFR Part 58 - GOOD LABORATORY PRACTICE FOR NONCLINICAL LABORATORY STUDIES

21 CFR Part 71 - COLOR ADDITIVE PETITIONS

21 CFR Part 99 - DISSEMINATION OF INFORMATION ON UNAPPROVED/NEW USES FOR MARKETED DRUGS, BIOLOGICS, AND DEVICES

21 CFR Part 310 - NEW DRUGS

21 CFR Part 570 - FOOD ADDITIVES

21 CFR Part 571 - FOOD ADDITIVE PETITIONS

21 CFR Part 610 - GENERAL BIOLOGICAL PRODUCTS STANDARDS

21 CFR Part 660 - ADDITIONAL STANDARDS FOR DIAGNOSTIC SUBSTANCES FOR LABORATORY TESTS

21 CFR Part 807 - ESTABLISHMENT REGISTRATION AND DEVICE LISTING FOR MANUFACTURERS AND INITIAL IMPORTERS OF DEVICES

21 CFR Part 809 - IN VITRO DIAGNOSTIC PRODUCTS FOR HUMAN USE

21 CFR Part 812 - INVESTIGATIONAL DEVICE EXEMPTIONS

21 CFR Part 814 - PREMARKET APPROVAL OF MEDICAL DEVICES

21 CFR Part 820 - QUALITY SYSTEM REGULATION

21 CFR Part 860 - MEDICAL DEVICE CLASSIFICATION PROCEDURES

21 CFR Part 861 - PROCEDURES FOR PERFORMANCE STANDARDS DEVELOPMENT

21 CFR Part 862 - CLINICAL CHEMISTRY AND CLINICAL TOXICOLOGY DEVICES

21 CFR Part 864 - HEMATOLOGY AND PATHOLOGY DEVICES

21 CFR Part 866 - IMMUNOLOGY AND MICROBIOLOGY DEVICES

21 CFR Part 868 - ANESTHESIOLOGY DEVICES

21 CFR Part 870 - CARDIOVASCULAR DEVICES

21 CFR Part 872 - DENTAL DEVICES

21 CFR Part 874 - EAR, NOSE, AND THROAT DEVICES

21 CFR Part 876 - GASTROENTEROLOGY-UROLOGY DEVICES

21 CFR Part 878 - GENERAL AND PLASTIC SURGERY DEVICES

21 CFR Part 880 - GENERAL HOSPITAL AND PERSONAL USE DEVICES

21 CFR Part 882 - NEUROLOGICAL DEVICES

21 CFR Part 884 - OBSTETRICAL AND GYNECOLOGICAL DEVICES

21 CFR Part 886 - OPHTHALMIC DEVICES

21 CFR Part 888 - ORTHOPEDIC DEVICES

21 CFR Part 890 - PHYSICAL MEDICINE DEVICES

21 CFR Part 892 - RADIOLOGY DEVICES

 

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