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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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