CONPHAR LATEX FOLEY CATH-STERILE

Catheter, Urological

CONPHAR, INC.

The following data is part of a premarket notification filed by Conphar, Inc. with the FDA for Conphar Latex Foley Cath-sterile.

Pre-market Notification Details

Device IDK792109
510k NumberK792109
Device Name:CONPHAR LATEX FOLEY CATH-STERILE
ClassificationCatheter, Urological
Applicant CONPHAR, INC. 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 Received1979-10-25
Decision Date1979-11-16

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