Section 1 Short title
This Act may be cited as the “Medical Device Electronic Labeling Act”.
Medical Device Electronic Labeling Act
A BILL
To amend the Federal Food, Drug, and Cosmetic Act to expand the types of devices for which required labeling may be made available solely by electronic means.
Sec. 2 Allowing required labeling of devices to be made available solely by electronic means
Section 502(f) of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 352(f)) is amended by striking “prescription devices intended for use in health care facilities or by a health care professional and required labeling for in vitro diagnostic devices intended for use by health care professionals or in blood establishments” and inserting “devices (including in vitro diagnostic devices)”.