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

TRANSLUMBAR AORTOGRAPHY NEEDLE CATHETER

K Number: K884375 · Decision Jan 11, 1989
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
24
Applicant Total
27
Review Days
85

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Basic Information

Device Name
TRANSLUMBAR AORTOGRAPHY NEEDLE CATHETER
K Number
K884375
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1300
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Argon Medical Corp.
Date Received
October 18, 1988
Decision Date
January 11, 1989
Product Code
DQR
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
DQR Cannula, Catheter

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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
K882221 OVER THE NEEDLE CATHETER, ARTERIAL CATHETER NEEDLE
K871297 KADIR HI-TORQUE GUIDE WIRE
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
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