KLIGLER IRON AGAR

Culture Media, Non-selective And Differential

ACUMEDIA MANUFACTURERS, INC.

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

Pre-market Notification Details

Device IDK833213
510k NumberK833213
Device Name:KLIGLER IRON AGAR
ClassificationCulture Media, Non-selective And Differential
Applicant ACUMEDIA MANUFACTURERS, INC. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeJSH  
CFR Regulation Number866.2320 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1983-09-19
Decision Date1983-10-27

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