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H.R. 7253

Clarifying Remanufacturing to Protect Patient Safety Act of 2022

Clarifying Remanufacturing to Protect Patient Safety Act of 2022

This bill specifies that entities that remanufacture medical devices in a manner that could change the performance or safety specifications or the intended use of the device must register with the Food and Drug Administration as producers of medical devices and comply with related requirements.

Referred to the Subcommittee on Health.

Rep. Peters, Scott H. [D-CA-52](D-CA)Sponsor
3 cosponsors2 D1 R
3cosponsors1committees4actions
  1. Committee

    Referred to the Subcommittee on Health.

    Health Subcommittee
  2. IntroReferralH11100

    Referred to the House Committee on Energy and Commerce.

    Energy and Commerce Committee
  3. IntroReferralIntro-H

    Introduced in House

  4. IntroReferral1000

    Introduced in House

Clarifying Remanufacturing to Protect Patient Safety Act of 2022 — Informed