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  1. Dec 22, 2023 · For the most up-to-date version of CFR Title 21, go to the Electronic Code of Federal Regulations (eCFR). New Search. Help | More About 21CFR. [Code of Federal Regulations] [Title 21, Volume 8]...

  2. The Electronic Code of Federal Regulations. Title 21. Displaying title 21, up to date as of 5/02/2024. Title 21 was last amended 4/29/2024. view historical versions. Title 21. Chapter I. Subchapter H. Part 801. Subpart A. § 801.1. Previous. Next. Top. § 801.1 Medical devices; name and place of business of manufacturer, packer or distributor.

  3. 21 CFR §801 Labeling - Code of Federal Regulations. '; PART 801. CFR. ›. Title 21. ›. Volume 8. ›. Chapter I. ›. Subchapter H. ›. Part 801 - Labeling. PART 801 - LABELING Authority: 21 U.S.C. 321, 331, 351, 352, 360d, 360i, 360j, 371, 374. Source: 41 FR 6896, Feb. 13, 1976, unless otherwise noted.

  4. www.fda.gov › medical-devices › overview-device-regulationDevice Labeling | FDA

    Labeling regulations pertaining to medical devices are found in the following Parts of Title 21 of the Code of Federal Regulations (CFR). General Device Labeling - 21 CFR Part 801. Use...

  5. Dec 22, 2023 · TITLE 21--FOOD AND DRUGS. CHAPTER I--FOOD AND DRUG ADMINISTRATION. DEPARTMENT OF HEALTH AND HUMAN SERVICES. SUBCHAPTER H - MEDICAL DEVICES. Subpart A - General Labeling Provisions. Sec. 801.1...

  6. Dec 22, 2023 · TITLE 21--FOOD AND DRUGS. CHAPTER I--FOOD AND DRUG ADMINISTRATION. DEPARTMENT OF HEALTH AND HUMAN SERVICES. SUBCHAPTER H - MEDICAL DEVICES. PART 801. LABELING. Subpart D - Exemptions...

  7. View the PDF for 21 CFR Part 801 Subpart A; These links go to the official, published CFR, which is updated annually. As a result, it may not include the most recent changes applied to the CFR. Learn more.

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