Much-criticised FDA medical device approvals get external review
The Food and Drug Administration is asking the government’s top medical advisers to review its system for approving certain types of medical devices, which has been criticized by safety advocates and government watchdogs. The nonprofit Institute of Medicine will conduct a two-year review of FDA’s so-called 510k review procedure, which allows device companies to quickly launch products similar to those already on the market.
The announcement Wednesday garnered approval from lawmakers on Capitol Hill who have been skeptical of the FDA program. “I have long been concerned that the 510k process permits too many devices on the market about whose safety and effectiveness even the FDA is uncertain,” said Rep. Henry Waxman. “The result is hundreds of recalls of important devices for serious safety concerns.”
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