BRUCELLA AGAR MODIFIED

Culture Media, Non-selective And Non-differential

ACUMEDIA MANUFACTURERS, INC.

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

Pre-market Notification Details

Device IDK833299
510k NumberK833299
Device Name:BRUCELLA AGAR MODIFIED
ClassificationCulture Media, Non-selective And Non-differential
Applicant ACUMEDIA MANUFACTURERS, INC. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeJSG  
CFR Regulation Number866.2300 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1983-09-22
Decision Date1983-11-07

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