FDA 510(k) Applications Submitted by SUZANNE 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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