BILL • US HOUSE
To amend the Federal Food, Drug, and Cosmetic Act to authorize requiring the manufacturers of a covered device to disclose to a patient all patient-specific data that is recorded or transmitted by the device and accessible to the manufacturer, and for other purposes.
119th Congress
Introduced by
Mikie Sherrill,
HR 6117 requires medical device makers to disclose all patient-specific data their devices collect and transmit to manufacturers, increasing transparency of health data practices.
Introduced in House
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