DESERET SUBCLAVIAN JUGULAR CATH-SET

Catheter, Intravascular, Therapeutic, Short-term Less Than 30 Days

WARNER-LAMBERT CO.

The following data is part of a premarket notification filed by Warner-lambert Co. with the FDA for Deseret Subclavian Jugular Cath-set.

Pre-market Notification Details

Device IDK833091
510k NumberK833091
Device Name:DESERET SUBCLAVIAN JUGULAR CATH-SET
ClassificationCatheter, Intravascular, Therapeutic, Short-term Less Than 30 Days
Applicant WARNER-LAMBERT CO. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeFOZ  
CFR Regulation Number880.5200 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1983-09-12
Decision Date1983-11-21

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