Last synced on 14 November 2025 at 11:06 pm

EpiZact

Page Type
Cleared 510(K)
510(k) Number
K233056
510(k) Type
Traditional
Applicant
GuideStar Medical Devices
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
11/2/2023
Days to Decision
38 days
Submission Type
Summary

EpiZact

Page Type
Cleared 510(K)
510(k) Number
K233056
510(k) Type
Traditional
Applicant
GuideStar Medical Devices
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
11/2/2023
Days to Decision
38 days
Submission Type
Summary