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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.
 
DeviceAXSYM HBSAG
Generic NameTest, Hepatitis B (B Antigen, B Surface Antigen, Be Antigen)
Regulation Number866.3172
ApplicantAbbott Laboratories, Inc.
100 Abbott Park Rd.
Dept. 9va-Ap8-1
Abbott Park, IL 60064
PMA NumberP050049
Supplement NumberS010
Date Received02/06/2012
Decision Date03/01/2012
Withdrawal Date11/15/2013
Product Code LOM 
Advisory Committee Microbiology
Supplement Type30-Day Notice
Supplement Reason Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review Granted? No
Combination ProductNo
Predetermined Change Control Plan AuthorizedNo
Approval Order Statement  
CHANGE TO THE TWO MICROBIAL TESTING METHODS FOR BIOBURDEN AND STERILITY DETERMINATION FOR CODE 37199 AND 97218.
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