HR 3203 · 112th Congress 2011โ€“2013, ended

Novel Device Regulatory Relief Act of 2011

Latest action · Oct 18, 2011 Referred to the Subcommittee on Health.

Progress

Where this bill reached, and when. A stage with no date was not reached; one that failed a vote and later carried shows the date it carried.

  1. IntroducedOct 14, 2011
  2. Passed HouseNot reached
  3. Passed SenateNot reached
  4. To the PresidentNot reached
  5. Became lawNot reached

Summary

Novel Device Regulatory Relief Act of 2011 - Amends the Federal Food, Drug, and Cosmetic Act to revise the process for requesting classification for a type of medical device that has not been previously classified by removing the requirement that a person can only file a request for classification of a new medical device after the Secretary of Health and Human Services (HHS) classifies the device as a class III device in response to the person filing a notice of intent to market the device.

Cosponsors 18

Members who signed on, in the order they did. Signatures ran from Oct 14, 2011 to Apr 24, 2012; 11 are original cosponsors, there from the day it was introduced.

SeatCosponsorSigned on
R-KYBrett GuthrieOriginalOct 14, 2011
R-PACharles W. DentOriginalOct 14, 2011
R-FLCliff StearnsOriginalOct 14, 2011
R-CADuncan HunterOriginalOct 14, 2011
R-MNErik PaulsenOriginalOct 14, 2011
R-ILJohn ShimkusOriginalOct 14, 2011
R-NJLeonard LanceOriginalOct 14, 2011
D-CALois CappsOriginalOct 14, 2011
R-TNMarsha BlackburnOriginalOct 14, 2011
R-TXMichael C. BurgessOriginalOct 14, 2011
R-OHRobert E. LattaOriginalOct 14, 2011
R-TXJohn Abney CulbersonOct 24, 2011
R-ORGreg WaldenNov 1, 2011
R-CAKen CalvertNov 1, 2011
R-SCMick MulvaneyJan 18, 2012
R-INTodd RokitaJan 23, 2012
D-UTJim MathesonFeb 1, 2012
R-AZPaul A. GosarApr 24, 2012

Committees 1

Where it was sent and what each committee and subcommittee did with it, in order.

ChamberCommitteeWhat it did
HouseEnergy and Commerce Committee
Referred Oct 14, 2011
Health Subcommittee
Referred Oct 18, 2011

Actions 3

Everything that happened, newest first.

  1. Oct 18, 2011Referred to the Subcommittee on Health.
  2. Oct 14, 2011Introduced in House
  3. Oct 14, 2011Referred to the House Committee on Energy and Commerce.

Research

What has been written about this bill: committee reports, cost estimates, the sponsor’s authority statement, printed hearings and the Congressional Research Service’s work.

Constitutional authority

Congress has the power to enact this legislation pursuant to the following: Article 1, Section 8 of the United States Constitution which states that Congress has the power to make all laws which shall be necessary and proper for carrying into execution the foregoing powers, and all other powers vested by this Constitution in the government of the United States, or in any department or officer thereof.

The sponsor’s statement, as printed in the page H6977.

Titles 2

Every title it has carried, official and short, at each stage.

Official Title as Introduced
To amend section 513 of the Federal Food, Drug, and Cosmetic Act to expedite the process for requesting de novo classification of a device.
Short Titles as Introduced
Novel Device Regulatory Relief Act of 2011

Subjects

Assigned by the Library of Congress. Policy area: Health.

Text 1

Each version as it was printed, newest first.

  1. Oct 14, 2011Introduced in House

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Everything here is as published by Congress: the summary is the Congressional Research Service's, the action wording is the clerks', and the subjects are the Library of Congress's. How far it got is read from the actions themselves, taking the most recent one of each kind, so a bill that failed a vote and later passed is shown as having passed. Records come from this bill on Congress.gov and govinfo.gov; cost estimates are the Congressional Budget Office's, and the hearings are the printed hearings GovInfo publishes, which can appear months after the hearing.