RPMI 1640 MEDIUM

Media And Components, Synthetic Cell And Tissue Culture

DUTCHLAND LABORATORIES, INC.

The following data is part of a premarket notification filed by Dutchland Laboratories, Inc. with the FDA for Rpmi 1640 Medium.

Pre-market Notification Details

Device IDK810767
510k NumberK810767
Device Name:RPMI 1640 MEDIUM
ClassificationMedia And Components, Synthetic Cell And Tissue Culture
Applicant DUTCHLAND LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeKIT  
CFR Regulation Number864.2220 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1981-03-23
Decision Date1981-05-08

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