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U.S. Department of Health and Human Services

Premarket Approval (PMA)
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Note: This medical device record is a PMA supplement. A supplement may have changed the device description/function or indication from that approved in the original PMA. Be sure to look at the original PMA record for more information.
 
DeviceVITEK LOMEFLOXACIN
Generic NameSusceptibility test cards, antimicrobial
Regulation Number866.1640
ApplicantBiomerieux Vitek, Inc.
595 Anglum Dr.
Hazelwood, MO 63042
PMA NumberN50510
Supplement NumberS063
Date Received08/08/1994
Decision Date11/16/1995
Reclassified Date12/28/2001
Product Code LTW 
Advisory Committee Microbiology
Supplement TypeNormal 180 Day Track
Supplement Reason Change Design/Components/Specifications/Material
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
Approval Order Statement  
APPROVAL FOR THE ADDITION OF THE ANTIMICROBIAL LOMOFLOXACIN OT THE VITEK GRAM NEGATIVE ANTIMICROBIAL PANELS
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