Last synced on 25 January 2026 at 3:41 am

AQUILION PRIME, V6.00

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K141741
510(k) Type
Traditional
Applicant
Toshibamedical Systems Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/26/2014
Days to Decision
152 days
Submission Type
Summary

AQUILION PRIME, V6.00

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K141741
510(k) Type
Traditional
Applicant
Toshibamedical Systems Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/26/2014
Days to Decision
152 days
Submission Type
Summary