MULTI-DRUG INFUSION SYSTEM

Pump, Infusion

I-FLOW CORP.

The following data is part of a premarket notification filed by I-flow Corp. with the FDA for Multi-drug Infusion System.

Pre-market Notification Details

Device IDK901978
510k NumberK901978
Device Name:MULTI-DRUG INFUSION SYSTEM
ClassificationPump, Infusion
Applicant I-FLOW CORP. 2532 WHITE RD. Irvine,  CA  92714
ContactRobert J Bard
CorrespondentRobert J Bard
I-FLOW CORP. 2532 WHITE RD. Irvine,  CA  92714
Product CodeFRN  
CFR Regulation Number880.5725 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1990-05-02
Decision Date1990-09-28

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