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

VSI MICRO-INTRODUCER SETS (REGULAR, STIFFEN), MODELS 7197V-7209V, 7240V-7256V, 7259V, 7230V, 7231V, 7260V, 7274V

K Number: K101604 · Decision Jan 24, 2011
Classifications
1
FEI Numbers
273
Registration Numbers
273
Same Product Code
701
Applicant Total
103
Review Days
230

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Basic Information

Device Name
VSI MICRO-INTRODUCER SETS (REGULAR, STIFFEN), MODELS 7197V-7209V, 7240V-7256V, 7259V, 7230V, 7231V, 7260V, 7274V
K Number
K101604
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Vascular Solutions, Inc.
Date Received
June 8, 2010
Decision Date
January 24, 2011
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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Other Clearances by Vascular Solutions, Inc.

K Number Device Name
K182232 Octane Mechanical Thrombectomy System
K181647 Bandit guidewire
K180913 VSI Micro-Introducer Kit
K180088 TrapLiner catheter
K180128 Warrior 14 guidewire
K173891 Gel-Bead (600-800 micron) - 1 ml sphere volume, Gel-Bead (600-800 micron) - 2 ml sphere volume
K173532 Raider Guidewire
K173266 Octane aspiration system
K170544 Langston dual lumen catheter
K171946 Gel-Bead
Search all 103 clearances from Vascular Solutions, Inc. →