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eCFR :: 21 CFR Chapter I Subchapter H -- Medical Devices
- https://www.ecfr.gov/current/title-21/chapter-I/subchapter-H
- Title 21. Displaying title 21, up to date as of 2/08/2023. Title 21 was last amended 2/02/2023. There have been changes in the last two weeks to Subchapter H. Food and Drug Administration, Department of Health and Human Services. Applicability. Performance …
eCFR :: 21 CFR Part 803 -- Medical Device Reporting
- https://www.ecfr.gov/current/title-21/chapter-I/subchapter-H/part-803
- You must submit your annual report to FDA, CDRH, Medical Device Reporting, P.O. Box 3002, Rockville, MD 20847-3002. Your annual report must include: ( 1) Your CMS …
eCFR :: 21 CFR Part 820 -- Quality System Regulation
- https://www.ecfr.gov/current/title-21/chapter-I/subchapter-H/part-820
- Manufacturers of human cells, tissues, and cellular and tissue-based products (HCT/Ps), as defined in § 1271.3(d) of this chapter, that are medical devices (subject to premarket …
Code of Federal Regulations (CFR) | FDA
- https://www.fda.gov/medical-devices/overview-device-regulation/code-federal-regulations-cfr
- Most of FDA's medical device and radiation-emitting product regulations are in Title 21 CFR Parts 800-1299. These final regulations codified in the CFR cover various aspects of …
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