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Business · 30/06/2004

FDA Publishes List of Approved Premarket Approval Applications for Medical Devices

The FDA has made available safety and effectiveness summaries for premarket approval applications (PMAs) of medical devices regulated by the Center for Biologics Evaluation and Research (CBER), providing public access to this information through the Internet and FDA's Division of Dockets Management.

Original source language: Federal Register — Food and Drug AdministrationOpen original release →

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