CLAVE CONNECTOR

Set, Administration, Intravascular

ICU MEDICAL, INC.

The following data is part of a premarket notification filed by Icu Medical, Inc. with the FDA for Clave Connector.

Pre-market Notification Details

Device IDK915571
510k NumberK915571
Device Name:CLAVE CONNECTOR
ClassificationSet, Administration, Intravascular
Applicant ICU MEDICAL, INC. 142 TECHNOLOGY DR. Irvine,  CA  92718
ContactAraceli C.fancher
CorrespondentAraceli C.fancher
ICU MEDICAL, INC. 142 TECHNOLOGY DR. Irvine,  CA  92718
Product CodeFPA  
CFR Regulation Number880.5440 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1991-12-12
Decision Date1992-09-21

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