Carefusion 209, Inc. is one of 21371 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Carefusion 209, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CAREFUSION NICOLET EDX, CAREFUSION NICOLET EDX, TECA ELITE DISPOSABLE CONCENTRIC NEEDLES
5
Total
5
Cleared
0
Denied
Carefusion 209, Inc. has 5 FDA 510(k) cleared medical devices. Based in Middleton, US.
Historical record: 5 cleared submissions from 2011 to 2012. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Carefusion 209, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Carefusion 209, Inc.
5 devices
Cleared
Apr 25, 2012
CAREFUSION NICOLET EDX
Neurology
23d
Cleared
Mar 15, 2012
CAREFUSION NICOLET EDX
Neurology
241d
Cleared
Aug 12, 2011
TECA ELITE DISPOSABLE CONCENTRIC NEEDLES
Neurology
28d
Cleared
Jun 17, 2011
TECA (TM) ELITE DISPOSABLE MONOPOLAR NEEDLES
Neurology
57d
Cleared
Apr 08, 2011
NICOLET WIRELESS EEG
Neurology
165d