INOX IV STAND

Stand, Infusion

BROADWEST CORP.

The following data is part of a premarket notification filed by Broadwest Corp. with the FDA for Inox Iv Stand.

Pre-market Notification Details

Device IDK852300
510k NumberK852300
Device Name:INOX IV STAND
ClassificationStand, Infusion
Applicant BROADWEST CORP. 260 WEST BROADWAY New York,  NY  10013
ContactJack Donovan
CorrespondentJack Donovan
BROADWEST CORP. 260 WEST BROADWAY New York,  NY  10013
Product CodeFOX  
CFR Regulation Number880.6990 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1985-05-29
Decision Date1985-06-20

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