FEELEY-GORMAN 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 Feeley-gorman Agar.

Pre-market Notification Details

Device IDK833301
510k NumberK833301
Device Name:FEELEY-GORMAN 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 Received1983-09-22
Decision Date1983-10-28

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