Carefusion 209, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K120979CAREFUSION NICOLET EDXApril 25, 2012
K112052CAREFUSION NICOLET EDXMarch 15, 2012
K112034TECA ELITE DISPOSABLE CONCENTRIC NEEDLESAugust 12, 2011
K111131TECA (TM) ELITE DISPOSABLE MONOPOLAR NEEDLESJune 17, 2011
K103140NICOLET WIRELESS EEGApril 8, 2011