FDA 510(k) Applications Submitted by DAIKEN MEDICAL CO, LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K071694 06/20/2007 COOPDECH ENDOBRONCHIAL BLOCKER TUBE, MODELS BBT-A30XXX, BBT-B30XXX DAIKEN MEDICAL CO, LTD.
K093888 12/18/2009 COOPDECH ENDOBRONCHIAL BLOCKER TUBE DAIKEN MEDICAL CO, LTD.


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