Minimed, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Minimed, Inc. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Minimed, Inc. has 9 FDA 510(k) cleared medical devices. Based in Sylmar, US.
Historical record: 9 cleared submissions from 2000 to 2003. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Minimed, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Minimed, Inc.
9 devices
Cleared
Nov 18, 2003
PARADIGMPAL, MODEL MMT-7330
General Hospital
186d
Cleared
Jul 23, 2003
MEDTRONIC MINIMED PARADIGM INSULIN PUMP, MODEL MMT-712
General Hospital
82d
Cleared
Jun 17, 2003
MEDTRONIC MINIMED PARADIGM MODEL 512 INSULIN PUMP AND THE BD PARADIGM LINK...
General Hospital
118d
Cleared
Aug 06, 2002
MEDTRONIC MINIMED COMLINK, HARDWARE MODEL 7304 & SOFTWARE MODEL 7311
General Hospital
50d
Cleared
Apr 05, 2001
MIMIMED SIL-SERTER INFUSION SET INSERTION SYSTEM, MODEL 385
General Hospital
56d
Cleared
Aug 18, 2000
PARADIGM SOF-SET MICRO QR, MODELS 324 AND 325
General Hospital
63d
Cleared
Aug 18, 2000
PARADIGM 1.5ML RESERVOIR, MODEL 326
General Hospital
63d
Cleared
Aug 18, 2000
MINIMED PARADIGM INSULIN PUMP, MODEL 511
General Hospital
63d
Cleared
Aug 18, 2000
PARADIGM SOF-SET ULTIMATE QR, MODELS 317 AND 318
General Hospital
63d