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

MiniMed 780G Insulin Pump (MMT-1884); MiniMed 780G Insulin Pump Kit (MMT-1894)

K Number: K253470 · Decision Jan 15, 2026
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
27
Applicant Total
8
Review Days
97

Basic Information

Device Name
MiniMed 780G Insulin Pump (MMT-1884); MiniMed 780G Insulin Pump Kit (MMT-1894)
K Number
K253470
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5730
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medtronic Minimed, Inc.
Date Received
October 10, 2025
Decision Date
January 15, 2026
Product Code
QFG
Advisory Committee
Clinical Chemistry
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
QFG Alternate Controller Enabled Insulin Infusion Pump

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