LEGIONELLA MWY SELECTIVE SUPPLEMENT

Supplement, Culture Media

OXOID U.S.A., INC.

The following data is part of a premarket notification filed by Oxoid U.s.a., Inc. with the FDA for Legionella Mwy Selective Supplement.

Pre-market Notification Details

Device IDK840331
510k NumberK840331
Device Name:LEGIONELLA MWY SELECTIVE SUPPLEMENT
ClassificationSupplement, Culture Media
Applicant OXOID U.S.A., INC. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeJSK  
CFR Regulation Number866.2450 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1984-01-25
Decision Date1984-05-11

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