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FDA 510(k) Applications Submitted by CAREFUSION 209, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K120979
04/02/2012
CAREFUSION NICOLET EDX
CAREFUSION 209, INC.
K111131
04/21/2011
TECA (TM) ELITE DISPOSABLE MONOPOLAR NEEDLES
CAREFUSION 209, INC.
K112034
07/15/2011
TECA ELITE DISPOSABLE CONCENTRIC NEEDLES
CAREFUSION 209, INC.
K112052
07/18/2011
CAREFUSION NICOLET EDX
CAREFUSION 209, INC.
K103140
10/25/2010
NICOLET WIRELESS EEG
CAREFUSION 209, INC.
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