FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

MEDTRONIC MINIMED PARADIGM INSULIN PUMP, MODEL MMT-712

K Number: K031390 · Decision Jul 23, 2003
Classifications
1
FEI Numbers
71
Registration Numbers
71
Same Product Code
74
Applicant Total
9
Review Days
82

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Basic Information

Device Name
MEDTRONIC MINIMED PARADIGM INSULIN PUMP, MODEL MMT-712
K Number
K031390
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5725
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Minimed, Inc.
Date Received
May 2, 2003
Decision Date
July 23, 2003
Product Code
LGZ
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LGZ Warmer, Thermal, Infusion Fluid

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LGZ), ordered by most recent decision date.

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Other Clearances by Minimed, Inc.

K Number Device Name
K031541 PARADIGMPAL, MODEL MMT-7330
K030531 MEDTRONIC MINIMED PARADIGM MODEL 512 INSULIN PUMP AND THE BD PARADIGM LINK GLUCOSE METER
K021974 MEDTRONIC MINIMED COMLINK, HARDWARE MODEL 7304 & SOFTWARE MODEL 7311
K010377 MIMIMED SIL-SERTER INFUSION SET INSERTION SYSTEM, MODEL 385
K001827 PARADIGM SOF-SET MICRO QR, MODELS 324 AND 325
K001829 MINIMED PARADIGM INSULIN PUMP, MODEL 511
K001832 PARADIGM SOF-SET ULTIMATE QR, MODELS 317 AND 318
K001828 PARADIGM 1.5ML RESERVOIR, MODEL 326