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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 NameABBOTT REALTIME HBV ASSAY
Classification Namehepatitis viral b dna detection
ApplicantABBOTT MOLECULAR, INC.
PMA NumberP080026
Supplement NumberS002
Date Received07/05/2011
Decision Date11/30/2011
Product Code
MKT[ Registered Establishments with MKT ]
Advisory Committee Microbiology
Supplement Type135 review track for 30-day notice
Supplement Reason process change: manufacturing
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Approval for a raw material change for two of the microvials used to manufacture the reagent components in the abbott realtime hbv amplification kit within the abbott realtime hbv assay.
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