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

MINIMED PARADIGM INSULIN PUMP, MODEL 511

K Number: K001829 · Decision Aug 18, 2000
Classifications
1
FEI Numbers
149
Registration Numbers
149
Same Product Code
847
Applicant Total
9
Review Days
63

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Basic Information

Device Name
MINIMED PARADIGM INSULIN PUMP, MODEL 511
K Number
K001829
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
June 16, 2000
Decision Date
August 18, 2000
Product Code
FRN
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
FRN Pump, Infusion

Similar 510(k) Clearances

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Other Clearances by Minimed, Inc.

K Number Device Name
K031541 PARADIGMPAL, MODEL MMT-7330
K031390 MEDTRONIC MINIMED PARADIGM INSULIN PUMP, MODEL MMT-712
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
K001832 PARADIGM SOF-SET ULTIMATE QR, MODELS 317 AND 318
K001828 PARADIGM 1.5ML RESERVOIR, MODEL 326