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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.
 
DeviceABBOTT AXSYM AUSAB
Generic NameTest, Hepatitis B (B Antigen, B Surface Antigen, Be Antigen)
Regulation Number866.3172
ApplicantAbbott Laboratories, Inc.
100 Abbott Park Rd.
Dept 9va- Ap5-2
Abbott Park, IL 60064
PMA NumberP060003
Supplement NumberS005
Date Received06/11/2010
Decision Date06/09/2011
Withdrawal Date11/15/2013
Product Code LOM 
Advisory Committee Microbiology
Supplement TypeReal-Time Process
Supplement Reason Change Design/Components/Specifications/Material
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
Approval Order Statement  
APPROVAL FOR CHANGES TO THE MANUFACTURING AND QUALITY CONTROL TESTING FOR AXSYM AUSAB CALIBRATORS, CONTROLS, AND REAGENTS.
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