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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name reagents, clostridium difficile toxin
510(k) Number K091109
Device Name XPERT C. DIFFICILE
Applicant
CEPHEID
904 CARIBBEAN DRIVE
SUNNYVALE,  CA  94089 -1189
Applicant Contact RUSSEL K ENNS
Correspondent
CEPHEID
904 CARIBBEAN DRIVE
SUNNYVALE,  CA  94089 -1189
Correspondent Contact RUSSEL K ENNS
Regulation Number866.2660
Classification Product Code
LLH  
Date Received04/16/2009
Decision Date 07/09/2009
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Microbiology
510k Review Panel Microbiology
Summary Summary
FDA Review Decision Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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