LETHEEN AGAR

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 Letheen Agar.

Pre-market Notification Details

Device IDK881543
510k NumberK881543
Device Name:LETHEEN AGAR
ClassificationCulture Media, Non-selective And Non-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 CodeJSG  
CFR Regulation Number866.2300 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1988-04-08
Decision Date1988-04-18

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.