Nipro Diabetes Systems, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nipro Diabetes Systems, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Nipro Diabetes Systems, Inc. has 5 FDA 510(k) cleared medical devices. Based in Lexington, US.
Historical record: 5 cleared submissions from 2001 to 2007. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Nipro Diabetes Systems, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Nipro Diabetes Systems, Inc.
5 devices
Cleared
Dec 14, 2007
AMIGO INSULIN PUMP
General Hospital
184d
Cleared
May 09, 2005
AMIGO INSULIN PUMP
General Hospital
90d
Cleared
Jun 26, 2002
GLUCOPRO SYRINGE, MODEL GPSY-XXXXXXXX
General Hospital
194d
Cleared
Jun 24, 2002
GLUCOPRO EVO INFUSION PUMP
General Hospital
263d
Cleared
May 08, 2001
GLUCOPRO INFUSION SET, MODEL GPISXXXXXXXX SERIES
General Hospital
26d