FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇰 Denmark

Lunderquist Extra Stiff Wire Guide

K Number: K251596 · Decision Nov 9, 2025
Classifications
1
FEI Numbers
257
Registration Numbers
258
Same Product Code
763
Applicant Total
18
Review Days
166

Basic Information

Device Name
Lunderquist Extra Stiff Wire Guide
K Number
K251596
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.1330
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
William Cook Europe Aps
Date Received
May 27, 2025
Decision Date
November 9, 2025
Product Code
DQX
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
DQX Wire, Guide, Catheter

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K211874 Günther Tulip Vena Cava Filter Set for Femoral Vein Approach, Günther Tulip Vena Cava Filter Set for Jugular Vein Approach, Günther Tulip Vena Cava Filter Set for Femoral and Jugular Vein Approach
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K172584 Günther Tulip Vena Cava Filter Set for Femoral Vein Approach, Günther Tulip Vena Cava Filter Set for Femoral and Jugular Vein Approach
K172557 Gunther Tulip Vena Cava Filter Set for Femoral Vein Approach, Gunther Tulip Vena Cava Filter Set for Jugular Vein Approach, Gunther Tulip Vena Cava Filter Set for Femoral and Jugular Vein Approach
K171712 Cook Celect Platinum Vena Cava Filter Set for Femoral Vein Approach, Cook Celect Platinum Vena Cava Filter Set for Jugular Vein Approach, Cook Celect Platinum Vena Cava Filter Set for Femoral and Jugular Vein Approach
K161813 Frova Intubating Introducer
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