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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name dna-reagents, mycobacterium spp.
510(k) Number K896493
Device Name ACCUPROBE MYCOBACTERIUM TUBERCULOSIS COMPLEX TEST
Original Applicant
GEN-PROBE, INC.
9880 campus point dr.
san diego,  CA  92121
Original Contact bruni, phd
Regulation Number866.3370
Classification Product Code
LQF  
Date Received11/13/1989
Decision Date 04/11/1990
Decision substantially equivalent (SE)
Classification Advisory Committee Microbiology
Review Advisory Committee Microbiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
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