Last synced on 25 April 2025 at 11:05 pm

CARTO VIZIGO® 8.5F Bi-Directional Guiding Sheath (D-1385-01-S, D-1385-02-S, D-1385-03-S)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231412
510(k) Type
Special
Applicant
Biosense Webster, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/10/2023
Days to Decision
55 days
Submission Type
Summary

CARTO VIZIGO® 8.5F Bi-Directional Guiding Sheath (D-1385-01-S, D-1385-02-S, D-1385-03-S)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231412
510(k) Type
Special
Applicant
Biosense Webster, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/10/2023
Days to Decision
55 days
Submission Type
Summary