Posted 09 April 2012
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.
'12 briefing held medical device notification
More Breaking News from RegLink