FDA 510(k) Applications Submitted by COLLEEN A KISTLER

FDA 510(k) Number Submission Date Device Name Applicant
K113021 10/11/2011 TRUFREEZE SYSTEM, TRUFREEZE SPRAY KIT CSA MEDICAL, INC.
K022133 07/01/2002 BD DIRECTIGEN EZ RSV KIT BECTON DICKINSON & CO.
K052481 09/09/2005 BD VIPER SYSTEM BECTON, DICKINSON & CO.
K033861 12/12/2003 BD PROBETEC ET LEGIONELLA PNEUMOPHILA (LP) AMPLIFIED DNA ASSAY BECTON, DICKINSON & CO.


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