United States · Bill · HR
H.R. 1494 (110th)
Pediatric Medical Device Safety and Improvement Act of 2007
Introduced
13 March 2007
Last action
14 March 2007 · Referred
Status
Referred to the Subcommittee on Health.
Sponsors
Sen. Markey, Edward J. [D-MA], Rep. Rogers, Mike J. [R-MI-8], Rep. Ramstad, Jim [R-MN-3], Rep. Capps, Lois [D-CA-24], Rep. Eshoo, Anna G. [D-CA-18], Rep. Grijalva, Raúl M. [D-AZ-7]
Subjects
Healthcare
Source updated
5 December 2025
Summary
Pediatric Medical Device Safety and Improvement Act of 2007 - Amends the Federal Food, Drug, and Cosmetic Act to require an application for the approval of a medical device or a product development protocol to include: (1) a description of any pediatric subpopulations that suffer from the disease or condition that the device is intended to treat, diagnose, or cure; and (2) the number of affected pediatric patients. Excludes a medical device distributed pursuant to the humanitarian device exemption from the prohibition that no device be sold for an amount that exceeds the cost of the device if: (1) the device is intended for the treatment or diagnosis of a disease or condition that occurs in pediatric patients; and (2) other specified requirements are met. Requires the Director of the National Institutes of Health (NIH) to designate a contact point to help innovators and physicians access funding for pediatric medical device development. Requires the Secretary of Health and Human Services to award grants for demonstration projects to promote pediatric device development. Includes as a duty of the Office of Pediatric Therapeutics increasing pediatric access to medical devices. Allows the Secretary to require: (1) postmarket surveillance on certain devices that are expected to have significant use in pediatric populations; and (2) a prospective surveillance period of more than 36 months for such devices, as necessary. Requires the Secretary, acting through the Commissioner of Food and Drugs, to establish a publicly accessible database of all studies and surveillance of medical devices.
This text is taken from the official record. PoliticalRepo does not editorialize.
Timeline
13 March 2007
Introduced
Referred to the House Committee on Energy and Commerce.
Source: IntroReferral
13 March 2007
Introduced
Introduced in House
Source: IntroReferral
13 March 2007
Introduced
Introduced in House
Source: IntroReferral
14 March 2007
Referred
Referred to the Subcommittee on Health.
Source: Committee
Votes
No vote records are attached yet.
Versions
- Introduced in House · 13 March 2007 · Download file
Documents
3 official files
Introduced in House (text)
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Introduced in House (text)
Introduced in House · EN · 13 March 2007
Introduced in House (PDF)
Introduced in House · EN · 13 March 2007
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Introduced in House
summary · EN · 13 March 2007
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Sponsors
- Sen. Markey, Edward J. [D-MA] · D · Sponsor
- Rep. Rogers, Mike J. [R-MI-8] · R · Sponsor
- Rep. Ramstad, Jim [R-MN-3] · R · Cosponsor
- Rep. Capps, Lois [D-CA-24] · D · Cosponsor
- Rep. Eshoo, Anna G. [D-CA-18] · D · Cosponsor
- Rep. Grijalva, Raúl M. [D-AZ-7] · D · Cosponsor
- · hsif00 · Standing
Related records
Sources
PoliticalRepo is an index and interpretation layer, not the authoritative legal source.
- Official source: https://www.congress.gov/bill/110th-congress/house-bill/1494
- Open data entity: https://api.congress.gov/v3/bill/110/hr/1494
- us · 110-hr-1494 · source updated 5 December 2025