Last synced on 14 November 2025 at 11:06 pm

LASSO NAV CATHETER

Page Type
Cleared 510(K)
510(k) Number
K093376
510(k) Type
Traditional
Applicant
Biosense Webster, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/18/2010
Days to Decision
232 days
Submission Type
Summary

LASSO NAV CATHETER

Page Type
Cleared 510(K)
510(k) Number
K093376
510(k) Type
Traditional
Applicant
Biosense Webster, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/18/2010
Days to Decision
232 days
Submission Type
Summary