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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.
Classification Namesusceptibility test cards, antimicrobial
Generic Nameantimicrobial susceptibility test system-short incubation
Regulation Number866.1640
PMA NumberN50510
Supplement NumberS135
Date Received04/06/2000
Decision Date06/21/2000
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 the antibiotic ceftriaxone at concentrations of 0. 06, 0. 25, 0. 5, and 1 microgram/ml to the vitek(r) 2 s. Pneumoniae susceptibility test system. The device as modified, will be marketed under the trade name vitek(r) 2 s. Pneumoniae susceptibility testing of streptococcus pneumoniae to ceftriaxone in the range of ,+0. 06 to >=4 micrograms/ml.