FDA 510(k) Applications Submitted by ACTIVAERO AMERICA, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K080100 01/14/2008 WATCHHALER ACTIVAERO AMERICA, INC.
K090730 03/19/2009 AKITA JET ACTIVAERO AMERICA, INC.
K072019 07/23/2007 AKITA2 APIXNEB ACTIVAERO AMERICA, INC.


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