Risk-Based Classification of Accessories Act of 2017

referredUnited States· United States Congress· EN

Introduced

25 April 2017

Last action

28 April 2017 · Referred

Status

Referred to the Subcommittee on Health.

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

25 April 2017
Introduced
Referred to the House Committee on Energy and Commerce.
Source: IntroReferral
25 April 2017
Introduced
Introduced in House
Source: IntroReferral
25 April 2017
Introduced
Introduced in House
Source: IntroReferral
28 April 2017
Referred
Referred to the Subcommittee on Health.
Source: Committee

Votes

No vote records are attached yet.

Versions

Introduced in House · 25 April 2017 · Download file

Documents

3 official files

Introduced in House (text)

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Introduced in House (text)
Introduced in House · EN · 25 April 2017
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Introduced in House (PDF)
Introduced in House · EN · 25 April 2017
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Introduced in House
summary · EN · 25 April 2017
Open at official source
Leesvertaling
Vertaal dit document naar jouw taal. PoliticalRepo bewaart geen aparte kopie per EU-taal.
Vertaal naar
Documentvertaling op verzoek met downloadbare PDF (logo + link naar de officiële bron). Het bronbestand blijft leidend.

Related records

related to ← Realizing Intended Safety for Certain Accessories Act of 2017

Sources

PoliticalRepo is an index and interpretation layer, not the authoritative legal source.

Official source: https://www.congress.gov/bill/115th-congress/house-bill/2144
Open data entity: https://api.congress.gov/v3/bill/115/hr/2144
us · 115-hr-2144 · source updated 11 August 2025