FDA 510(k) Applications Submitted by DIGIO2 INTERNATIONAL CO., LTD

FDA 510(k) Number Submission Date Device Name Applicant
K091430 05/14/2009 CARE PAL, MODEL CPW-10X DIGIO2 INTERNATIONAL CO., LTD
K133105 09/30/2013 BREEZE NEBULIZER (NBR-10X) DIGIO2 INTERNATIONAL CO., LTD


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