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April 9, 2012
by RAPS

Device Safety Reassessed

The Korean Food and Drug Administration (KFDA) held a briefing focused on the reassessment of the safety of devices based on 12 years marketing experience and consumer reports.

The briefing on 6 April covered devices such as radiation treatment devices, sutures, diagnostic devices, bio-monitoring equipment, treatment equipment and cardiovascular equipment.

Read more:
'12 briefing held medical device notification
More Breaking News from RegLink

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