Disetronic Medical Systems AG is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Disetronic Medical Systems AG - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Disetronic Medical Systems AG has 12 FDA 510(k) cleared general hospital devices. Based in Fort Myers, US.
Historical record: 12 cleared submissions from 2000 to 2010.
Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Disetronic Medical Systems AG
12 devices
Cleared
May 14, 2010
ACCU-CHEK FLEXLINK PLUS INFUSION SET, ACCU-CHECK LINKASSIST PLUS INSERTION...
General Hospital
63d
Cleared
Feb 21, 2007
ACCU-CHEK ULTRAFLEX INFUSION SET
General Hospital
30d
Cleared
Nov 27, 2006
ACCU-CHEK LINKASSIST
General Hospital
42d
Cleared
Jun 15, 2006
ACCU-CHEK INSULIN PUMP CONFIGURATION SOFTWARE (STANDARD), MODEL 04625137001
General Hospital
76d
Cleared
Mar 18, 2005
ACCU-CHEK SPIRIT
General Hospital
150d
Cleared
Dec 01, 2004
MODIFICATION TO D-TRONPLUS
General Hospital
30d
Cleared
Mar 09, 2004
ULTRAFLEX INFUSION SET
General Hospital
84d
Cleared
Oct 29, 2002
DISETRONIC H-TRONPLUS INSULIN INFUSION PUMP
General Hospital
14d
Cleared
Sep 11, 2002
MODIFICATION TO DISETRONIC D-TRONPLUS INSULIN INFUSION PUMP
General Hospital
16d
Cleared
Aug 02, 2002
DISETRONIC D-TRON INSULIN INFUSION PUMP
General Hospital
70d
Cleared
Feb 15, 2001
DISETRONIC RAPID SUBCUTANEOUS INFUSION SET AND DISTERONIC RAPID D...
General Hospital
55d
Cleared
Jun 21, 2000
DISETRONIC MULTIFUSE INFUSION PUMP SYSTEM
General Hospital
26d