SILICONE FOLEY CATHETER

Catheter, Retention Type, Balloon

COOK UROLOGICAL, INC.

The following data is part of a premarket notification filed by Cook Urological, Inc. with the FDA for Silicone Foley Catheter.

Pre-market Notification Details

Device IDK951106
510k NumberK951106
Device Name:SILICONE FOLEY CATHETER
ClassificationCatheter, Retention Type, Balloon
Applicant COOK UROLOGICAL, INC. 1100 WEST MORGAN ST. P.O. BOX 227 Spencer,  IN  47460
ContactDarcy Job
CorrespondentDarcy Job
COOK UROLOGICAL, INC. 1100 WEST MORGAN ST. P.O. BOX 227 Spencer,  IN  47460
Product CodeEZL  
CFR Regulation Number876.5130 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1995-03-10
Decision Date1995-05-25

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