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

SUBCUTANEOUS TUNNELING NEEDLES & HANDLES

K Number: K854327 · Decision Nov 13, 1985
Classifications
1
FEI Numbers
78
Registration Numbers
78
Same Product Code
7
Applicant Total
42
Review Days
16

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Basic Information

Device Name
SUBCUTANEOUS TUNNELING NEEDLES & HANDLES
K Number
K854327
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4200
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Concord Laboratories, Inc.
Date Received
October 28, 1985
Decision Date
November 13, 1985
Product Code
GCB
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
GCB Needle, Catheter

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Other Clearances by Concord Laboratories, Inc.

K Number Device Name
K883840 DRI-VENT ARTERIAL BLOOD SAMPLING KIT
K871825 MECONIUM SUCTION CATHETER
K864535 TRACHEOBRONCHIAL SUCTION CATHETER, CAT. NO. 6110
K862039 CONCORD CARE TRAY
K854601 SPRING GUIDE CATHETER ANESTHESIA CONDUCTION CATH
K851134 REGIONAL ANESTHESIA TRAYS
K842095 EPIDURAL TRAYS
K841486 ARTERIAL BLOOD SAMPLING KITS
K840986 PREFILLED PULSATOR SYRINGE
K840987 VAPORIZED HEPARIN
Search all 42 clearances from Concord Laboratories, Inc. →