Realizing Intended Safety for Certain Accessories Act of 2017

Summary

Risk-Based Classification of Accessories Act of 2017 This bill revises how accessories to medical devices are classified. Specifically, the Food and Drug Administration must classify accessories based on the risks when used as intended , notwithstanding the classification of any other device with which such accessory is intended to be used.

This text is taken from the official record. PoliticalRepo does not editorialize.

Timeline

1. 8 May 2017

   Introduced

   Introduced in Senate

   Source: IntroReferral

2. 8 May 2017

   Introduced

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

   Source: IntroReferral

Votes

No vote records are attached yet.

Versions

• Introduced in Senate · 8 May 2017 · Download file

Documents

3 official files

• Introduced in Senate (text)

  Introduced in Senate · EN · 8 May 2017

  ViewDownloadOpen at official source

• Introduced in Senate (PDF)

  Introduced in Senate · EN · 8 May 2017

  ViewDownloadOpen at official source

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  Vertaal document

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• Introduced in Senate

  summary · EN · 8 May 2017

  Open at official source

  Leesvertaling

  Vertaal dit document naar jouw taal. PoliticalRepo bewaart geen aparte kopie per EU-taal.

  Vertaal naarNL · DutchDE · GermanFR · FrenchES · SpanishIT · ItalianPL · PolishPT · PortugueseSV · SwedishDA · DanishFI · FinnishEL · GreekCS · CzechHU · HungarianRO · RomanianBG · BulgarianHR · CroatianSK · SlovakSL · SlovenianLT · LithuanianLV · LatvianET · EstonianGA · IrishMT · Maltese

  Vertaal document

  Documentvertaling op verzoek met downloadbare PDF (logo + link naar de officiële bron). Het bronbestand blijft leidend.

Sponsors

• Sen. Roberts, Pat [R-KS] · R · Sponsor
• Sen. Donnelly, Joe [D-IN] · D · Sponsor
• Sen. Burr, Richard [R-NC] · R · Sponsor
• · sshr00 · Standing

Related records

• related to → FDA Reauthorization Act of 2017
• related to → Risk-Based Classification of Accessories Act of 2017