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

VASCULAR SOLUTIONS SCLERO-KIT

K Number: K043019 · Decision Dec 1, 2004
Classifications
1
FEI Numbers
440
Registration Numbers
440
Same Product Code
687
Applicant Total
103
Review Days
28

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Basic Information

Device Name
VASCULAR SOLUTIONS SCLERO-KIT
K Number
K043019
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5570
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Vascular Solutions, Inc.
Date Received
November 3, 2004
Decision Date
December 1, 2004
Product Code
FMI
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
FMI Needle, Hypodermic, Single Lumen

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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. →