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

Transjugular Liver Access Sets

K Number: K171820 · Decision Mar 9, 2018
Classifications
1
FEI Numbers
268
Registration Numbers
268
Same Product Code
682
Applicant Total
118
Review Days
263

Basic Information

Device Name
Transjugular Liver Access Sets
K Number
K171820
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cook Incorporated
Date Received
June 19, 2017
Decision Date
March 9, 2018
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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