ALL PUPOSE URETHRAL CATHETER

Catheter, Urological

AMERICAN HOSPITAL SUPPLY CORP.

The following data is part of a premarket notification filed by American Hospital Supply Corp. with the FDA for All Pupose Urethral Catheter.

Pre-market Notification Details

Device IDK803080
510k NumberK803080
Device Name:ALL PUPOSE URETHRAL CATHETER
ClassificationCatheter, Urological
Applicant AMERICAN HOSPITAL SUPPLY CORP. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeKOD  
CFR Regulation Number876.5130 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1980-12-05
Decision Date1980-12-22

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