Last synced on 14 November 2025 at 11:06 pm

iCAC Device

Page Type
Cleared 510(K)
510(k) Number
K230223
510(k) Type
Traditional
Applicant
Bunkerhill, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/25/2023
Days to Decision
89 days
Submission Type
Summary

iCAC Device

Page Type
Cleared 510(K)
510(k) Number
K230223
510(k) Type
Traditional
Applicant
Bunkerhill, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/25/2023
Days to Decision
89 days
Submission Type
Summary