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FDA 510(k) Applications Submitted by SUZANNE M VOGEL
FDA 510(k) Number
Submission Date
Device Name
Applicant
K090301
02/06/2009
BINAXNOW PBP2A TEST, MODEL 890-000
BINAX, INC.
K090964
04/06/2009
BINAXNOX STAPHYLOCOCCUS AUREUS TEST
BINAX, INC.
K091766
06/17/2009
CLEARVIEW EXACT PBP2A TEST, MODEL 891-000
BINAX, INC.
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