Codan US Corp. is one of 15054 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Codan US Corp. - FDA 510(k) Cleared Devices
Recent clearances: CODAN SAFEFEED ENTERAL FEEDING RESERVOIR, IV ADMINISTRATION SET B400 SP, CODAN CHEMOSPIKE
7
Total
7
Cleared
0
Denied
Codan US Corp. has 7 FDA 510(k) cleared medical devices. Based in Irvine, US.
Historical record: 7 cleared submissions from 1999 to 2012. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Codan US Corp. 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 - Codan US Corp.
7 devices
Cleared
Mar 19, 2012
CODAN SAFEFEED ENTERAL FEEDING RESERVOIR
Gastroenterology & Urology
224d
Cleared
Oct 21, 2004
IV ADMINISTRATION SET B400 SP
General Hospital
21d
Cleared
Mar 04, 2004
IV ADMINISTRATION AND CONNECT SETS
General Hospital
142d
Cleared
Jun 27, 2002
EXTENSION SET LIGHT-SAFE, MODEL BC565
General Hospital
50d
Cleared
Mar 28, 2002
CODAN US I.V. ADMINISTRATION SET, MODEL B400 SP
General Hospital
140d
Cleared
Sep 07, 2000
I.V. SET-LUER LOCK WITH LATEX FREE INJECTION SITE, MODEL B411
General Hospital
79d
Cleared
Apr 13, 1999
CODAN CHEMOSPIKE
General Hospital
40d