Last synced on 14 November 2025 at 11:06 pm

DualView Catheter

Page Type
Cleared 510(K)
510(k) Number
K250751
510(k) Type
Traditional
Applicant
Terumo Corporation
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
7/17/2025
Days to Decision
127 days
Submission Type
Summary

DualView Catheter

Page Type
Cleared 510(K)
510(k) Number
K250751
510(k) Type
Traditional
Applicant
Terumo Corporation
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
7/17/2025
Days to Decision
127 days
Submission Type
Summary