Last synced on 14 November 2025 at 11:06 pm

TeraRecon Aorta.CT (1.1.0)

Page Type
Cleared 510(K)
510(k) Number
K243158
510(k) Type
Traditional
Applicant
TeraRecon, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/23/2025
Days to Decision
115 days
Submission Type
Summary

TeraRecon Aorta.CT (1.1.0)

Page Type
Cleared 510(K)
510(k) Number
K243158
510(k) Type
Traditional
Applicant
TeraRecon, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/23/2025
Days to Decision
115 days
Submission Type
Summary