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

Available versions
Introduced (House)View official text

1 version available

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Timeline

  1. Referred to the House Committee on Energy and Commerce.

    House of Representatives

  2. Introduced in House

  3. Referred to the Subcommittee on Health.

    House of Representatives

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