Medical Devices Approved by the FDA Can Still Be HarmfulSeveral high-risk medical devices, which were approved under a less stringent FDA approval process with no human testing, may be having serious side effects on individuals who received the devices.
May 21, 2011 /24-7PressRelease/ -- Before doctors and hospitals implant or use medical devices for patients, the Food and Drug Administration (FDA) must review the devices. The review process is called pre-market
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