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

TRAY, CATHETERIZATION W/ CATHETER

K Number: K760128 · Decision Oct 7, 1976
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
59
Applicant Total
42
Review Days
101

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Basic Information

Device Name
TRAY, CATHETERIZATION W/ CATHETER
K Number
K760128
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5130
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Concord Laboratories, Inc.
Date Received
June 28, 1976
Decision Date
October 7, 1976
Product Code
FCM
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
FCM Tray, Catheterization, Sterile Urethral, With Or Without Catheter (Kit)

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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
K854327 SUBCUTANEOUS TUNNELING NEEDLES & HANDLES
K851134 REGIONAL ANESTHESIA TRAYS
K842095 EPIDURAL TRAYS
K841486 ARTERIAL BLOOD SAMPLING KITS
K840986 PREFILLED PULSATOR SYRINGE
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