[Congressional Bills 108th Congress]
[From the U.S. Government Publishing Office]
[H.R. 2218 Referred in Senate (RFS)]

  1st Session
                                H. R. 2218


_______________________________________________________________________


                   IN THE SENATE OF THE UNITED STATES

                           November 20, 2003

                                Received

                            December 9, 2003

 Read twice and referred to the Committee on Health, Education, Labor, 
                              and Pensions

_______________________________________________________________________

                                 AN ACT


 
 To amend the Federal Food, Drug, and Cosmetic Act to provide for the 
  regulation of all contact lenses as medical devices, and for other 
                               purposes.

    Be it enacted by the Senate and House of Representatives of the 
United States of America in Congress assembled,

SECTION 1. FINDINGS.

    The Congress finds as follows:
            (1) All contact lenses have significant effects on the eye 
        and pose serious potential health risks if improperly 
        manufactured or used without appropriate involvement of a 
        qualified eye care professional.
            (2) Most contact lenses currently marketed in the United 
        States, including certain plano and decorative contact lenses, 
        have been approved as medical devices pursuant to premarket 
        approval applications or cleared pursuant to premarket 
        notifications by the Food and Drug Administration (``FDA'').
            (3) FDA has asserted medical device jurisdiction over most 
        corrective and noncorrective contact lenses as medical devices 
        currently marketed in the United States, including certain 
        plano and decorative contact lenses, so as to require approval 
        pursuant to premarket approval applications or clearance 
        pursuant to premarket notifications.
            (4) All contact lenses can present risks if used without 
        the supervision of a qualified eye care professional. Eye 
        injuries in children and other consumers have been reported for 
        contact lenses that are regulated by FDA as medical devices 
        primarily when used without professional involvement, and 
        noncorrective contact lenses sold without approval or clearance 
        as medical devices have caused eye injuries in children.

SEC. 2. REGULATION OF CERTAIN ARTICLES AS MEDICAL DEVICES.

    Section 520 of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 
360j) is amended by adding at the end the following subsection:

                ``Regulation of Contact Lens as Devices

    ``(n)(1) All contact lenses shall be deemed to be devices under 
section 201(h).
    ``(2) Paragraph 1 shall not be construed as having any legal effect 
on any article that is not described in that paragraph.''.

            Passed the House of Representatives November 19, 2003.

            Attest:

                                                 JEFF TRANDAHL,

                                                                 Clerk.