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IUD safety anger sparks FDA premarket talk
Congress faces pressure to require FDA clearance for intrauterine devices after gynecologists testified to higher pregnancy rates and serious complications. Lawmakers consider extending premarket testing to medical devices, with drug rules as a model, amid warnings from doctors and advocates about safety and effectiveness.
MENTIONED IN THIS ARTICLE
New York
Nyt
Congress
Federal Food and Drug Administration
FDA
House Intergovernmental Relations Subcommittee
Planned Parenthood World Federation
Russell J. Thomson
Army Medical Corps
Fort Polk la
Thomsen