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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 PMA supplement. A supplement may have changed the device description/function or indication from that approved in the original PMA. Be sure to look at the original PMA record for more information.
 
DeviceCOBAS AMPLIPREP/COBAS AMPLICOR HCV TEST, VERSION 2.0
Generic NameAssay, hybridization and/or nucleic acid amplification for detection of hepatitis c rna,hepatitis c virus
Regulation Number866.3170
ApplicantRoche Molecular Systems, Inc.
4300 HACIENDA DR.
PLEASANTON, CA 94588-0900
PMA NumberP000012
Supplement NumberS003
Date Received02/13/2004
Decision Date08/30/2004
Withdrawal Date 08/26/2016
Product Code MZP 
Advisory Committee Microbiology
Supplement TypeNormal 180 Day Track
Supplement Reason Change Design/Components/Specifications/Material
Expedited Review Granted? No
Combination ProductNo
Approval Order Statement  
APPROVAL FOR THE COBAS AMPLIPREP/ COBAS AMPLICOR HCV TEST, V2.0 INSTRUMENT WHICH FULLY AUTOMATES THE SPECIMEN TESTING PORTION OF THE TEST.
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