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FDA 510(k) Applications Submitted by COLLEEN 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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