Section 330 united center Section 330(b) makes it a crime to adulterate a medical device. A medical device is considered adulterated if it is manufactured, processed, packed, or held in conditions that do not comply with applicable regulations, or if it contains a substance that renders it harmful to users. Section 330(c) makes it a crime to forge or alter any certificate, label, or other document required by law to accompany a medical device. This subsection also applies to any person who fails to provide required documents or makes false statements in connection with the sale or distribution of a medical device. Section 330(d) makes it a crime to knowingly receive or conceal a medical device that is adulterated or misbranded, with the intent to defraud or mislead. This subsection also applies to any person who knowingly sells or transports a misbranded or adulterated medical device. * Evening (after 6 pm): .00 for adults, .00 for seniors and children The first subsection, Section 330(a), makes it a crime to introduce or deliver for introduction into interstate commerce any medical device that is misbranded. A medical device is considered misbranded if its labeling is false or misleading in any particular, or if it does not bear adequate directions for its use. This subsection also applies to any person who repacks or changes the labeling of a medical device in a way that makes it misbranded. Section 330(b) makes it a crime to adulterate a medical device. A medical device is considered adulterated if it is manufactured, processed, packed, or held in conditions that do not comply with applicable regulations, or if it contains a substance that renders it harmful to users. Extended Forecast It is important to note that Section 330 applies only to medical devices that are introduced or delivered for introduction into interstate commerce. This means that it does not apply to medical devices that are used solely within a single state. However, many medical devices are subject to regulation by both the federal government and the states, so it is important to ensure compliance with all applicable laws and regulations. In addition to Section 330, there are many other federal laws and regulations that govern the manufacture, sale, and distribution of medical devices. These laws and regulations are enforced by several different agencies, including the Food and Drug Administration (FDA), the Federal Trade Commission (FTC), and the Department of Justice (DOJ). The FDA is responsible for ensuring the safety and effectiveness of medical devices, and for regulating their labeling, advertising, and distribution. The FTC is responsible for enforcing truth-in-advertising laws and for preventing false or misleading advertising of medical devices. The DOJ is responsible for prosecuting criminal violations of federal laws, including those related to medical devices. In summary, Section 330 of the United States Criminal Code makes it a crime to misbrand or adulterate a medical device, to forge or alter required documents, or to knowingly receive or conceal a misbranded or adulterated medical device. Penalties for violating Section 330 can be severe, and there are many other federal laws and regulations that govern the manufacture, sale, and distribution of medical devices. It is important for manufacturers, distributors, and users of medical devices to ensure compliance with all applicable laws and regulations.