Considers a specified medical device to aid in breast self-examination to be a device for which a report required under the Federal Food, Drug, and Cosmetic Act prior to introduction into interstate commerce for commercial distribution has been accepted by the Secretary of Health and Human Services and which has been approved under such Act.
Introduced in House
Introduced in House
Referred to the House Committee on Commerce.
Referred to the Subcommittee on Health and Environment.
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