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AKITA2 APIXNEB

Page Type
Cleared 510(K)
510(k) Number
K072019
510(k) Type
Traditional
Applicant
ACTIVAERO AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/2007
Days to Decision
105 days
Submission Type
Summary

AKITA2 APIXNEB

Page Type
Cleared 510(K)
510(k) Number
K072019
510(k) Type
Traditional
Applicant
ACTIVAERO AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/2007
Days to Decision
105 days
Submission Type
Summary