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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.
 
Trade NameCOBAS TAQMAN HCV TEST V2.0 FOR USE WITH THE HIGH PURE SYSTEM
Classification Nameassay,hybridization and/or nucleic acid amplification for detection of hepatitis c rna,hepatitis c virus
ApplicantROCHE MOLECULAR SYSTEMS, INC.
PMA NumberP060030
Supplement NumberS015
Date Received02/08/2011
Decision Date02/24/2011
Product Code
MZP[ Registered Establishments with MZP ]
Advisory Committee Microbiology
Supplement Type30-day notice
Supplement Reason process change: manufacturing
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Elimination of the in-process chemical testing of the buffer concentrate component of the master mix used with the cobas taqman hcv test, v2. 0 within the fda approved pcr manufacturing center (pmc) facility in branchburg, new jersey.
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