LUER-LOK MULTIFLO ADAPTER

Set, Administration, Intravascular

DESERET MEDICAL, INC.

The following data is part of a premarket notification filed by Deseret Medical, Inc. with the FDA for Luer-lok Multiflo Adapter.

Pre-market Notification Details

Device IDK882797
510k NumberK882797
Device Name:LUER-LOK MULTIFLO ADAPTER
ClassificationSet, Administration, Intravascular
Applicant DESERET MEDICAL, INC. 9450 SOUTH STATE ST. Sandy,  UT  84070
ContactCharles J Welle
CorrespondentCharles J Welle
DESERET MEDICAL, INC. 9450 SOUTH STATE ST. Sandy,  UT  84070
Product CodeFPA  
CFR Regulation Number880.5440 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1988-07-06
Decision Date1988-07-18

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