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

Extended Reservoir; MiniMed Reservoir

K Number: K241622 · Decision Jul 2, 2024
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
83
Applicant Total
48
Review Days
27

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Basic Information

Device Name
Extended Reservoir; MiniMed Reservoir
K Number
K241622
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
880.5725
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medtronic Minimed
Date Received
June 5, 2024
Decision Date
July 2, 2024
Product Code
LZG
Advisory Committee
General Hospital
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
LZG Pump, Infusion, Insulin

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Other Clearances by Medtronic Minimed

K Number Device Name
K253701 SmartGuard Technology; Predictive Low Glucose Technology
K253512 MiniMed Go App
K242775 InPen System App (MMT-8060 (iOS), MMT-8061 (Android))
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
K052432 MEDTRONIC MINIMED PARADIGM LEAPFROG II INFUSION SET, MODELS MMT-802S1, MMT-802L1, MMT-802S2, MMT-802L2
Search all 48 clearances from Medtronic Minimed →