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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.
 
DeviceADVIA CENTAUR HEPATITIS B E ANTIGEN ASSAY
Generic NameTest, Hepatitis B (B Antigen, B Surface Antigen, Be Antigen)
Regulation Number866.3172
ApplicantSiemens Healthcare Diagnostics
511 Benedict Ave.
Tarrytown, NY 10591
PMA NumberP090024
Supplement NumberS001
Date Received05/05/2015
Decision Date10/18/2016
Reclassified Date10/20/2025
Product Code LOM 
Advisory Committee Microbiology
Supplement TypeNormal 180 Day Track
Supplement Reason Labeling Change - Indications/instructions/shelf life/tradename
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
Approval Order Statement  
Approval for the migration of the ADVIA Centaur® HBeAg Assay (ADVIA Centaur® HBeAg Assay and ADVIA Centaur® HBeAg Quality Control Material) to the ADVIA Centaur® XPT system.
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