H.R.1652 - Over-the-Counter Hearing Aid Act of 2017115th Congress (2017-2018)
|Sponsor:||Rep. Kennedy, Joseph P., III [D-MA-4] (Introduced 03/21/2017)|
|Committees:||House - Energy and Commerce|
|Latest Action:||House - 03/24/2017 Referred to the Subcommittee on Health. (All Actions)|
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Summary: H.R.1652 — 115th Congress (2017-2018)All Information (Except Text)
Introduced in House (03/21/2017)
Over-the-Counter Hearing Aid Act of 2017
This bill amends the Federal Food, Drug, and Cosmetic Act to require the Food and Drug Administration (FDA) to categorize certain hearing aids as over-the-counter hearing aids and issue regulations regarding those hearing aids. The regulations for over-the-counter hearing aids must: (1) provide reasonable assurances of safety and efficacy; (2) establish output limits and labeling requirements; and (3) describe requirements for the sale of hearing aids in-person, by mail, or online, without a prescription.
State and local governments may not establish or continue in effect requirements specifically applicable to hearing products that are not identical to FDA requirements and that restrict or interfere with the servicing or sale of over-the-counter hearing aids.
The FDA must update and finalize its draft guidance on hearing products. The guidance must clarify which products are medical devices.