Medical Device Electronic Labeling Act
United States118th CongressHR-3723House of Representatives
Updated: May 26, 2023
Summary
Medical Device Electronic Labeling Act This bill allows directions for use and warning labels for all medical devices to be provided electronically. Currently, this option extends only to (1) prescription devices that are used in health care facilities or by health care professionals, and (2) in vitro diagnostic devices that are used by health care professionals or in blood establishments.
Bill texts
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Timeline
Referred to the House Committee on Energy and Commerce.
House of Representatives
Introduced in House
Referred to the Subcommittee on Health.
House of Representatives
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