FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

ARGON CUT BIOPSY NEEDLES, VARIOUS SIZES

K Number: K853312 · Decision Sep 12, 1985
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
10
Applicant Total
27
Review Days
36

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Basic Information

Device Name
ARGON CUT BIOPSY NEEDLES, VARIOUS SIZES
K Number
K853312
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Argon Medical Corp.
Date Received
August 7, 1985
Decision Date
September 12, 1985
Product Code
DWO
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
DWO Needle, Biopsy, Cardiovascular

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K884375 TRANSLUMBAR AORTOGRAPHY NEEDLE CATHETER
K882221 OVER THE NEEDLE CATHETER, ARTERIAL CATHETER NEEDLE
K871297 KADIR HI-TORQUE GUIDE WIRE
K852880 PEEL-AWAY SHEATH(A COMPONENT OF ARGON INTROD SET)
K844555 PATHFINDER CARDIOVASCULAR CATHETER
K842039 ARGON DUAL LUMEN HEMODIALYSIS, CATHETER
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