Last synced on 20 May 2022 at 11:05 pm

AKITA2 APIXNEB

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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