Which action is considered a form of medical fraud?

Billing for experimental medical devices not approved by authorities constitutes a form of medical fraud because it involves charging for a service or product that has not undergone the necessary regulatory approvals and may not have been proven to be safe or effective. This action poses significant risks not only to patients but also undermines the integrity of the healthcare system. When providers bill for such devices, they are not only breaching ethical standards but also engaging in deceptive practices that can lead to serious legal repercussions.

Authorized billing for medical services, accurate documentation of patient visits, and providing free samples to patients are all legitimate practices that serve the interests of both healthcare providers and patients. These practices do not involve deceit or misrepresentation of the services or products being provided. Therefore, they do not fall into the category of fraud, distinguishing them clearly from the billing of unapproved experimental devices.