DESERET INTRACATH INTRAVENOUS CATHETER

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 Intracath Intravenous Catheter.

Pre-market Notification Details

Device IDK821372
510k NumberK821372
Device Name:DESERET INTRACATH INTRAVENOUS CATHETER
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 Received1982-05-10
Decision Date1982-06-02

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
20886333210163 K821372 000
20886333210156 K821372 000
20886333210149 K821372 000
20886333210132 K821372 000
20886333210125 K821372 000
20886333210118 K821372 000
20886333210101 K821372 000

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