XL AGAR BASE

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 Xl Agar Base.

Pre-market Notification Details

Device IDK881572
510k NumberK881572
Device Name:XL AGAR BASE
ClassificationCulture Media, Selective And Differential
Applicant ACUMEDIA MANUFACTURERS, INC. 3651 CLIPPER MILL RD. Baltimore,  MD  21211
ContactCunningham, Phd
CorrespondentCunningham, Phd
ACUMEDIA MANUFACTURERS, INC. 3651 CLIPPER MILL RD. Baltimore,  MD  21211
Product CodeJSI  
CFR Regulation Number866.2360 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1988-04-11
Decision Date1988-04-18

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