Carefusion 2200, Inc. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Carefusion 2200, Inc. has 12 FDA 510(k) cleared medical devices. Based in Waukegan, US.
Last cleared in 2021. Active since 2011.
Browse the FDA 510(k) cleared devices submitted by Carefusion 2200, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Carefusion 2200, Inc.
12 devices
Cleared
Mar 04, 2021
V. Mueller Cosgrove Flex Clamps, Model Number-CV1033, CV1061, CV1133, CV1161,...
Cardiovascular
28d
Cleared
May 04, 2017
Snowden-Pencer MicroLap 3mm Laparoscopic Instruments
General & Plastic Surgery
133d
Cleared
Jan 18, 2017
Multi-Link X2 ECG Cable and Lead Wire System
Cardiovascular
140d
Cleared
Aug 25, 2016
AirLife Autofill Humidification Chamber
Anesthesiology
157d
Cleared
Mar 21, 2016
Genesis Low Temperature Reusable Rigid Container System
General Hospital
98d
Cleared
Feb 01, 2016
Snowden-Pencer Ergonomic Take-Apart In-Line and Pistol Grip Laparoscopic...
General & Plastic Surgery
287d
Cleared
Jan 08, 2015
Genesis Reusable Rigid Container System
General Hospital
121d
Cleared
Aug 27, 2014
GENESIS REUSABLE RIGID CONTAINER SYSTEM
General Hospital
146d
Cleared
Apr 21, 2014
KAHN UTERINE CANNULA, JARCHO UTERINE CANNULA, NEAL FALLOPIAN CANNULA
Obstetrics & Gynecology
26d
Cleared
Sep 07, 2012
SNOWDEN PENCER LAPAROSCOPIC ERGONOMIC REPOSABLE SCISSORS
General & Plastic Surgery
294d
Cleared
Apr 27, 2012
GENESIS REUSABLE RIGID CONTAINER SYSTEM
General Hospital
239d
Cleared
May 06, 2011
DIAMOND-FLEX(R) GRASPERS
General & Plastic Surgery
98d