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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 Namesusceptibility test cards, antimicrobial
Regulation Number866.1640
595 anglum dr.
hazelwood, MO 63042-2395
PMA NumberN50510
Supplement NumberS134
Date Received04/06/2000
Decision Date06/14/2000
Product Code
LTW[ Registered Establishments with LTW ]
Advisory Committee Microbiology
Supplement Typenormal 180 day track
Supplement Reason change design/components/specifications/material
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Approval for the addition of the antibiotic erythromycin at concentrations of 0. 12, 0. 25 and 0. 5 micrograms/ml to the vitek(r) 2 s. Pneumoniae susceptibility test system. The device, as mofified, will be marketed under the trade name vitek(r) 2 s. Pneumoniae susceptibility test cards for use in the vitek(r) 2 system and is indicated for use for the susceptibility testing of streptococcus pneumoniae to erythromycin in the range of <=0. 06 to >=1 micrograms/ml.