Last synced on 14 November 2025 at 11:06 pm

ACTIVAPATCH

Page Type
Cleared 510(K)
510(k) Number
K091326
510(k) Type
Traditional
Applicant
ACTIVATEK INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/27/2009
Days to Decision
22 days
Submission Type
Summary

ACTIVAPATCH

Page Type
Cleared 510(K)
510(k) Number
K091326
510(k) Type
Traditional
Applicant
ACTIVATEK INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/27/2009
Days to Decision
22 days
Submission Type
Summary