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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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