CATHETER, URETHERAL

Catheter, Urological

C.R. BARD, INC.

The following data is part of a premarket notification filed by C.r. Bard, Inc. with the FDA for Catheter, Uretheral.

Pre-market Notification Details

Device IDK770814
510k NumberK770814
Device Name:CATHETER, URETHERAL
ClassificationCatheter, Urological
Applicant C.R. BARD, 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 Received1977-05-03
Decision Date1977-10-18

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