US HB3203 | 2011-2012 | 112th Congress
Status
October 18 2011 - Referred to the Subcommittee on Health.
Pending: House Subcommittee on Health Committee
Text: Latest bill text (Introduced) [PDF]
Pending: House Subcommittee on Health Committee
Text: Latest bill text (Introduced) [PDF]
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.
Title
Novel Device Regulatory Relief Act of 2011
Sponsors
History
| Date | Chamber | Action |
|---|---|---|
| 2011-10-18 | House | Referred to the Subcommittee on Health. |
| 2011-10-14 | House | Referred to the House Committee on Energy and Commerce. |
Subjects
Administrative remedies
Department of Health and Human Services
Drug safety, medical device, and laboratory regulation
Food and Drug Administration (FDA)
Health
Health technology, devices, supplies
Department of Health and Human Services
Drug safety, medical device, and laboratory regulation
Food and Drug Administration (FDA)
Health
Health technology, devices, supplies
US Congress State Sources
| Type | Source |
|---|---|
| Summary | http://thomas.loc.gov/cgi-bin/bdquery/z?d112:HN03203:@@@L&summ2=m& |
| Text | http://gpo.gov/fdsys/pkg/BILLS-112hr3203ih/pdf/BILLS-112hr3203ih.pdf |
