510(k) K253470

Device
MiniMed 780G Insulin Pump (MMT-1884); MiniMed 780G Insulin Pump Kit (MMT-1894)
Applicant
Medtronic Minimed, Inc.
510(k) number
K253470
Product code
QFG
Decision
Substantially Equivalent (SESE)
Decision date
2026-01-15
Date received
2025-10-10
Regulation
880.5730
Classification name
Alternate Controller Enabled Insulin Infusion Pump
Medical specialty
Clinical Chemistry
Review panel
Clinical Chemistry
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Amber Street
Address
18000 Devonshire St. Northridge CA US 91325 91325

FDA Registration Numbers

Source Documents

510(k) summary PDF

Other 510(k) Records For Product Code QFG

510(k)DeviceApplicantDecision date
K253976iLet ACE PumpBeta Bionics, Inc.2026-04-30
K253743MiniMed Flex pumpMedtronic Minimed, Inc.2026-03-12
K253074Tandem Mobi insulin pump with interoperable technologyTandem Diabetes Care, Inc.2025-11-06
K252770iLet ACE PumpBeta Bionics, Inc.2025-09-29
K250792t:slim X2 insulin pump with interoperable technologyTandem Diabetes Care, Inc.2025-09-24
K251032MiniMed 780G insulin pumpMedtronic Minimed, Inc.2025-07-01
K250930twiist systemDeka Research & Development Corp.2025-04-02
K234027embecta Insulin Delivery SystemEmbecta Medical I, LLC2024-08-30
K241078Tandem Mobi Insulin Pump with interoperable technologyTandem Diabetes Care, Inc.2024-07-26
K241178DEKA ACE Pump SystemDeka Research and Development2024-05-24
K240309Tandem Mobi insulin pump with interoperable technologyTandem Diabetes Care, Inc.2024-03-21
K233952DEKA ACE Pump SystemDeka Research and Development2024-03-13
K230545Inessa SystemTriple Jump Israel , Ltd.2023-12-20
K232380t:slim X2 Insulin Pump with Interoperable TechnologyTandem Diabetes Care, Inc.2023-11-03
K231826Omnipod 5 ACE PumpInsulet Corporation2023-10-18