BILE ESCULIN AGAR

Culture Media, Selective And Differential

ACUMEDIA MANUFACTURERS, INC.

The following data is part of a premarket notification filed by Acumedia Manufacturers, Inc. with the FDA for Bile Esculin Agar.

Pre-market Notification Details

Device IDK832572
510k NumberK832572
Device Name:BILE ESCULIN AGAR
ClassificationCulture Media, Selective And Differential
Applicant ACUMEDIA MANUFACTURERS, INC. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeJSI  
CFR Regulation Number866.2360 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1983-08-02
Decision Date1983-09-12

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