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

Rusch Simplastic Foley Catheters

K Number: K162989 · Decision Feb 24, 2017
Classifications
1
FEI Numbers
119
Registration Numbers
119
Same Product Code
127
Applicant Total
64
Review Days
120

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Basic Information

Device Name
Rusch Simplastic Foley Catheters
K Number
K162989
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5130
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Teleflexmedical, Inc.
Date Received
October 27, 2016
Decision Date
February 24, 2017
Product Code
EZL
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
EZL Catheter, Retention Type, Balloon

Similar 510(k) Clearances

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Other Clearances by Teleflexmedical, Inc.

K Number Device Name
K232469 Rüsch Latex Gold Foley Catheter
K212077 Teleflex Rusch SoftSimplastic Foley Catheters
K192324 Sheridan Spiral-Flex Endotracheal Tubes
K182847 Hudson RCI Voldyne Volumetric Exerciser
K181979 Rusch FloCath Quick 18 Fr. Coudé Hydrophilic Intermittent Catheter
K183461 Rusch Flocath Hydrophilic Intermittent Catheter, Rusch MMG Hydrophilic Intermittent Catheter
K181852 Percuvance Percutaneous Surgical System
K173280 Neonatal ConchaSmart Breathing Circuits
K172775 MiniLap System with MiniGrip Handle, MiniLap System with ThumbGrip Handle
K161770 Rusch Silicone Foley Catheter
Search all 64 clearances from Teleflexmedical, Inc. →