VITEK 2 GRAM POSITIVE QUINUPRISTIN/DALFOPRISTIN

System, Test, Automated, Antimicrobial Susceptibility, Short Incubation

BIOMERIEUX, INC.

The following data is part of a premarket notification filed by Biomerieux, Inc. with the FDA for Vitek 2 Gram Positive Quinupristin/dalfopristin.

Pre-market Notification Details

Device IDK032738
510k NumberK032738
Device Name:VITEK 2 GRAM POSITIVE QUINUPRISTIN/DALFOPRISTIN
ClassificationSystem, Test, Automated, Antimicrobial Susceptibility, Short Incubation
Applicant BIOMERIEUX, INC. 595 ANGLUM DR. Hazelwood,  MO  63042 -2320
ContactNancy Weaver
CorrespondentNancy Weaver
BIOMERIEUX, INC. 595 ANGLUM DR. Hazelwood,  MO  63042 -2320
Product CodeLON  
CFR Regulation Number866.1645 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2003-09-04
Decision Date2003-10-31
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
03573026356163 K032738 000

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