ClearanceBrief
Company ยท US

Nipro Diabetes Systems, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2001 to 2007. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
1recalls (0 in 12 months)
1recalls that name a 510(k)

Product codes

CodeDeviceRecords
LZGPump, Infusion, Insulin4
FMFSyringe, Piston1
FPASet, Administration, Intravascular1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Dec 14, 2007K071613AMIGO INSULIN PUMP
Nipro Diabetes Systems, Inc.
LZG
May 9, 2005K050312AMIGO INSULIN PUMP
Nipro Diabetes Systems, Inc.
LZG
Jun 26, 2002K014114GLUCOPRO SYRINGE, MODEL GPSY-XXXXXXXX
Nipro Diabetes Systems, Inc.
FMF
Jun 24, 2002K013309GLUCOPRO EVO INFUSION PUMP
Nipro Diabetes Systems, Inc.
LZG
May 8, 2001K011120GLUCOPRO INFUSION SET, MODEL GPISXXXXXXXX SERIES
Nipro Diabetes Systems, Inc.
FPA

Latest recalls

DateFirm and productCodeLinked 510(k)
Sep 14, 2004Nipro Diabetes Systems, Inc.
Amigo Insulin Infusion Pump
Terminated
LZGK013309
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