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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 HBE (RDNA) EIA
Generic NameTest, Hepatitis B (B Antigen, B Surface Antigen, Be Antigen)
Regulation Number866.3172
ApplicantAbbott Laboratories
100 Abbott Park Rd.
Dept:09va Bldg: Ap6c-2
Abbott Park, IL 60064
PMA NumberP790025
Supplement NumberS008
Date Received12/18/2002
Decision Date01/17/2003
Withdrawal Date03/22/2007
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  
CHANGES TO MANUFACTURING PROCESS, TEST METHOD ADDITIONS, AND SPECIFICATION CHANGES.
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