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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 supplement. The device description may have changed. Be sure to look at the original PMA to get an up-to-date view of this device.
 
Trade NameVITEK 2 SYSTEM
Classification Namesusceptibility test cards, antimicrobial
Generic Namesusceptibility test cards, antimicrobial
Regulation Number866.1640
ApplicantBIOMERIEUX VITEK, INC.
PMA NumberN50510
Supplement NumberS084
Date Received08/18/1998
Decision Date06/28/1999
Product Code
LTW[ Registered Establishments with LTW ]
Advisory Committee Microbiology
Supplement Typenormal 180 day track
Supplement Reason change design/components/specifications - other
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Approval for the addition of four antibiotics to the gram positive susceptibility card. The device as modified will be marketed under the trade name vitek(r) 2 system and is intended as a laboratory aid in the determination of the in vitro susceptibility of aerobic gram positive bacteria when tested on a gram positive susceptibility test card with specific antimicrobial agents and concentrations.
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