Last synced on 25 April 2025 at 11:05 pm

CARTO VIZIGO 8.5F Bi-Directional Guiding Sheath

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K170997
510(k) Type
Traditional
Applicant
Biosense Webster, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/25/2017
Days to Decision
113 days
Submission Type
Summary

CARTO VIZIGO 8.5F Bi-Directional Guiding Sheath

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K170997
510(k) Type
Traditional
Applicant
Biosense Webster, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/25/2017
Days to Decision
113 days
Submission Type
Summary