Animas Corp. is one of 21626 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Animas Corp. - FDA 510(k) Cleared Devices
Recent clearances: SYMPHONY GLUCOSE MANAGEMENT SYSTEM, EZ MANAGER MAX DIABETES MANAGEMENT SOFTWARE, EZMANAGER MAX DIABETES MANAGEMENT SOFTWARE
10
Total
10
Cleared
0
Denied
Animas Corp. has 10 FDA 510(k) cleared general hospital devices. Based in Frazer, US.
Historical record: 10 cleared submissions from 2000 to 2008.
Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Citech as regulatory consultant.
FDA 510(k) Regulatory Record - Animas Corp.
10 devices
Cleared
Jun 24, 2008
SYMPHONY GLUCOSE MANAGEMENT SYSTEM
General Hospital
110d
Cleared
May 15, 2008
EZ MANAGER MAX DIABETES MANAGEMENT SOFTWARE
General Hospital
73d
Cleared
Mar 30, 2007
EZMANAGER MAX DIABETES MANAGEMENT SOFTWARE
General Hospital
109d
Cleared
Dec 10, 2004
ANIMAS MODEL IR1250 INSULIN INFUSION PUMP
General Hospital
53d
Cleared
Oct 16, 2003
MODEL IR 1200 INSULIN PUMP
General Hospital
86d
Cleared
Jun 05, 2003
EZMANAGER PLUS
General Hospital
317d
Cleared
Jun 04, 2002
ANIMUS EZSERTER INFUSION SET INSERTER
General Hospital
12d
Cleared
May 29, 2002
MODEL R1000 IR INSULIN PUMP, EZLINK SOFTWARE, SERMON SOFTWARE, R1000 IR...
General Hospital
23d
Cleared
Aug 27, 2001
EZ SET INFUSION SET
General Hospital
11d
Cleared
Feb 10, 2000
R1000 SERIES INSULIN PUMP
General Hospital
140d