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Next Generation Access Catheter

Page Type
Cleared 510(K)
510(k) Number
K234074
510(k) Type
Traditional
Applicant
Balt USA, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/2/2024
Days to Decision
193 days
Submission Type
Summary

Next Generation Access Catheter

Page Type
Cleared 510(K)
510(k) Number
K234074
510(k) Type
Traditional
Applicant
Balt USA, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/2/2024
Days to Decision
193 days
Submission Type
Summary