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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name nucleic acid amplification assay system, group b streptococcus, direct specimen test
510(K) Number K062948
Device Name SMART GBS AND SMARTCYCLE DX SYSTEM AND SOFTWARE, VERSION 1.7B
Applicant
CEPHEID
904 caribbean drive
sunnyvale,  CA  94089 1189
Contact russel k enns
Regulation Number866.3740
Classification Product Code
NJR  
Date Received09/28/2006
Decision Date 12/08/2006
Decision substantially equivalent - CLIA submission (CS)
Classification Advisory Committee Microbiology
Review Advisory Committee Microbiology
summary summary
FDA Review Decision Summary
Type Traditional
Reviewed by Third Party No
Expedited Review No
Combination Product No
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