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

MEDTRONIC MINIMED PARADIGM RESERVOIR, MODEL MMT-332

K Number: K032005 · Decision Aug 22, 2003
Classifications
1
FEI Numbers
149
Registration Numbers
149
Same Product Code
847
Applicant Total
48
Review Days
53

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Basic Information

Device Name
MEDTRONIC MINIMED PARADIGM RESERVOIR, MODEL MMT-332
K Number
K032005
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5725
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medtronic Minimed
Date Received
June 30, 2003
Decision Date
August 22, 2003
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

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Other Clearances by Medtronic Minimed

K Number Device Name
K253701 SmartGuard Technology; Predictive Low Glucose Technology
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K242775 InPen System App (MMT-8060 (iOS), MMT-8061 (Android))
K241622 Extended Reservoir; MiniMed Reservoir
K160860 MiniMed Quick-serter
K120206 MEDTRONIC MINIMED PARADIGM INSULIN PUMPS
K100432 POLYFIN INFUSION SET, MODELS MMT-165, MMT-365, MMT-366, MMT-312S AND MMT-312L AND SOF-SET INFUSION SETS
K073356 PARADIGM INSULIN INFUSION PUMP, MODELS MMT-512, MMT-712, MMT-515 AND MMT-715
K053177 MEDTRONIC MINIMED PARADIGM INSULIN PUMP, MODEL MMT-712E
K052431 MEDTRONIC MINIMED LEAPFROG II INFUSION SET, MODELS MMT-801S1, MMT-801L1, MMT-801S2, MMT-801L2, MMT-803S1
Search all 48 clearances from Medtronic Minimed →