Monthly Archives: January 2016

DXE Medical PMA Series – Part 2: Affected Devices

fda

FDA’s new stringent evaluation standards are set to improve dependability of automated external defibrillators (AEDs).

This is part 2 of the DXE Medical PMA Series regarding important information you should know about the FDA’s recent change in regulations on AED Pre-Market Approval (PMA) requirements. Continue reading

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