AGAR PLATE XLD

Culture Media, Non-selective And Differential

OTISVILLE BIOTECH, INC.

The following data is part of a premarket notification filed by Otisville Biotech, Inc. with the FDA for Agar Plate Xld.

Pre-market Notification Details

Device IDK832532
510k NumberK832532
Device Name:AGAR PLATE XLD
ClassificationCulture Media, Non-selective And Differential
Applicant OTISVILLE BIOTECH, 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 Received1983-07-29
Decision Date1983-09-29

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