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

PEEL-AWAY SHEATH(A COMPONENT OF ARGON INTROD SET)

K Number: K852880 · Decision Aug 29, 1985
Classifications
1
FEI Numbers
273
Registration Numbers
273
Same Product Code
701
Applicant Total
27
Review Days
51

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Basic Information

Device Name
PEEL-AWAY SHEATH(A COMPONENT OF ARGON INTROD SET)
K Number
K852880
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Argon Medical Corp.
Date Received
July 9, 1985
Decision Date
August 29, 1985
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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K884375 TRANSLUMBAR AORTOGRAPHY NEEDLE CATHETER
K882221 OVER THE NEEDLE CATHETER, ARTERIAL CATHETER NEEDLE
K871297 KADIR HI-TORQUE GUIDE WIRE
K853312 ARGON CUT BIOPSY NEEDLES, VARIOUS SIZES
K844555 PATHFINDER CARDIOVASCULAR CATHETER
K842039 ARGON DUAL LUMEN HEMODIALYSIS, CATHETER
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