FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

CARTO VIZIGO 8.5F Bi-Directional Guiding Sheath

K Number: K170997 · Decision Jul 25, 2017
Classifications
1
FEI Numbers
268
Registration Numbers
268
Same Product Code
682
Applicant Total
20
Review Days
113

Basic Information

Device Name
CARTO VIZIGO 8.5F Bi-Directional Guiding Sheath
K Number
K170997
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biosense Webster, Inc.
Date Received
April 3, 2017
Decision Date
July 25, 2017
Product Code
DYB
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DYB Introducer, Catheter

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