380 PIGGYBACK CONTROLLER

Controller, Infusion, Intravascular, Electronic

IMED CORP.

The following data is part of a premarket notification filed by Imed Corp. with the FDA for 380 Piggyback Controller.

Pre-market Notification Details

Device IDK823026
510k NumberK823026
Device Name:380 PIGGYBACK CONTROLLER
ClassificationController, Infusion, Intravascular, Electronic
Applicant IMED CORP. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeLDR  
CFR Regulation Number880.5725 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1982-10-14
Decision Date1982-11-22

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