Disetronic Medical Systems is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Disetronic Medical Systems - FDA 510(k) Cleared Devices
17
Total
13
Cleared
0
Denied
Disetronic Medical Systems has 13 FDA 510(k) cleared general hospital devices. Based in Minnetonka, US.
Historical record: 13 cleared submissions from 1991 to 2001.
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
17 devices
Cleared
Nov 20, 2001
DISETRONIC PENFINE INSULIN INJECTION PEN NEEDLE
General Hospital
6d
Cleared
Dec 30, 1999
DISETRONIC D-TRON INSULIN INFUSION PUMP
General Hospital
20d
Cleared
Dec 29, 1999
DISENTRONIC PENFINE INJECTION PEN NEEDLE
General Hospital
16d
Cleared
Nov 22, 1999
DISETRONIC PEN P100
General Hospital
21d
Cleared
Jun 15, 1999
DAHEDI INSULIN INFUSION PUMP
General Hospital
55d
Cleared
Feb 12, 1999
DISETRONIC MULTIFUSE INFUSION PUMP SYSTEM
General Hospital
16d
Cleared
Oct 19, 1998
DISETRONIC PEN
General Hospital
55d
Cleared
Aug 06, 1998
DISETRONIC PENFINE INJECTION PEN NEEDLE
General Hospital
27d
Cleared
Sep 24, 1997
DISETRONIC PENFINE INJECTION PEN NEEDLE
General Hospital
19d
Cleared
Sep 15, 1997
DISETRONIC H-TRON PLUS V 100 INSULIN INFUSION PUMP
General Hospital
31d
Cleared
Jan 30, 1997
DISETRONIC D-MODEM
General Hospital
255d
Cleared
May 24, 1996
DISETRONIC MULTIFUSE PUMP SYSTEM
General Hospital
217d