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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 NameIMX(R) HAVAB
Classification Namehepatitis a test (antibody and igm antibody)
Generic Nameantibody to hepatitis a virus 125i (human)
Regulation Number866.3310
ApplicantABBOTT LABORATORIES
PMA NumberP780012
Supplement NumberS008
Date Received02/06/1998
Decision Date05/12/1998
Product Code
LOL[ Registered Establishments with LOL ]
Advisory Committee Microbiology
Supplement Type Special Supplement
Supplement Reason labeling change - instructions
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Approval for the abbott imx(r) havab(r). This device is indicated for the qualitative determiantion of total antibody to heaptitis a antigen in human serum or plasma.
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