The Code of Federal Regulations is the codification of the general and permanent rules published in the Federal Register by the executive departments and agencies of the Federal Government.

This print ISBN is the U.S. Federal Government Official edition of this title. 21 CFR Parts 800 to 1299 covers the U. S. Food and Drug Administration within the U.S. Department of Health and Human Services. Within this volume, you will find rules, procedures, and regulations pertaining to medical devices, such as cardiovascular devices, dentistry devices, orthopedic, gastroenterology-urology, in vitro, anestheology, and more. Plus, you will find rules, procedures, and regulations relating to mammography quality standards, radiological health, tobacco products, cigarette package advertising warnings, cigarettes and smokeless tobacco, human tissue intended for transplantation, and more. Audiences: medical device producers and marketers, medical practitioners, tobacco proudcers andmarketers, human health researchers and practioners. Healthcare device manufacturers, hosptital radiological and other medical technicians and departments, physicians, nurses, out-patient clinics' personnel, and healthcare policy advocates, tobacco producers and advertisers/marketers as well as human health researchers and practitionersmay be interested in this volume."

Includes the decisions of the Supreme Courts of Massachusetts, Ohio, Indiana, and Illinois, and Court of Appeals of New York; May/July 1891-Mar./Apr. 1936, Appellate Court of Indiana; Dec. 1926/Feb. 1927-Mar./Apr. 1936, Courts of Appeals of Ohio.