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

KADIR HI-TORQUE GUIDE WIRE

K Number: K871297 · Decision Apr 10, 1987
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
237
Applicant Total
27
Review Days
10

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Basic Information

Device Name
KADIR HI-TORQUE GUIDE WIRE
K Number
K871297
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5130
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Argon Medical Corp.
Date Received
March 31, 1987
Decision Date
April 10, 1987
Product Code
KOD
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
KOD Catheter, Urological

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Other Clearances by Argon Medical Corp.

K Number Device Name
K904994 CLOSED SYSTEM FLUSH SET
K895511 CATHETER BALLOON DILATOR PRESSURE GAUGE
K894157 OBTURATOR
K891022 INTRODUCER FOR PTCA GUIDING CATHETERS
K884375 TRANSLUMBAR AORTOGRAPHY NEEDLE CATHETER
K882221 OVER THE NEEDLE CATHETER, ARTERIAL CATHETER NEEDLE
K853312 ARGON CUT BIOPSY NEEDLES, VARIOUS SIZES
K852880 PEEL-AWAY SHEATH(A COMPONENT OF ARGON INTROD SET)
K844555 PATHFINDER CARDIOVASCULAR CATHETER
K842039 ARGON DUAL LUMEN HEMODIALYSIS, CATHETER
Search all 27 clearances from Argon Medical Corp. →