Last synced on 14 November 2025 at 11:06 pm

IMAGEN3D

Page Type
Cleared 510(K)
510(k) Number
K122241
510(k) Type
Traditional
Applicant
CARDIOVASCULAR IMAGING TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/24/2012
Days to Decision
89 days
Submission Type
Summary

IMAGEN3D

Page Type
Cleared 510(K)
510(k) Number
K122241
510(k) Type
Traditional
Applicant
CARDIOVASCULAR IMAGING TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/24/2012
Days to Decision
89 days
Submission Type
Summary