FDA 510(k)

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

K-Number: K253470 · 2026-01-15

Decision Date2026-01-15

Product CodeQFG

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

MiniMed 780G Insulin Pump (MMT-1884); MiniMed 780G Insulin Pump Kit (MMT-1894) is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Minimed, Inc.. It received FDA 510(k) clearance on 2026-01-15 under 510(k) number K253470. The device is classified under product code QFG. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MiniMed 780G Insulin Pump (MMT-1884); MiniMed 780G Insulin Pump Kit (MMT-1894)?

MiniMed 780G Insulin Pump (MMT-1884); MiniMed 780G Insulin Pump Kit (MMT-1894) is a medical device that received FDA 510(k) clearance on 2026-01-15. The listed applicant is Medtronic Minimed, Inc.. The 510(k) number is K253470.

When did MiniMed 780G Insulin Pump (MMT-1884); MiniMed 780G Insulin Pump Kit (MMT-1894) receive FDA 510(k) clearance?

MiniMed 780G Insulin Pump (MMT-1884); MiniMed 780G Insulin Pump Kit (MMT-1894) received FDA 510(k) clearance on 2026-01-15, under 510(k) number K253470.

Who is the listed applicant for MiniMed 780G Insulin Pump (MMT-1884); MiniMed 780G Insulin Pump Kit (MMT-1894)?

The FDA 510(k) record lists Medtronic Minimed, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MiniMed 780G Insulin Pump (MMT-1884); MiniMed 780G Insulin Pump Kit (MMT-1894)?

The FDA product code for MiniMed 780G Insulin Pump (MMT-1884); MiniMed 780G Insulin Pump Kit (MMT-1894) is QFG.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT04414280The Impact of Hybrid Closed-loop Insulin Delivery in Type 1 Diabetes on Glycemic Control and PROMsACTIVE_NOT_RECRUITING NCT07720388Supporting Medtronic 780G Insulin Pump Adoption in Latino Patients: A Spanish - Language Training InitiativeNOT_YET_RECRUITING NCT06739811Clinical Evaluation of the Medtronic Implantable Insulin Pump System (MIIPS 2020) in Adult Subjects With Type 1 Diabetes (CIP347)RECRUITING NCT07227805Evaluation of the Safety and Performance of the Novel Medtronic Experimental Automated Insulin Delivery System (NMX8) in People Living With Diabetes (NEXUS)RECRUITING NCT07228117GATEWAY: Safety Evaluation of the MiniMed™ NMX8-AID System in Children and Adults Living With DiabetesRECRUITING NCT07408141MiniMed Fit Payload Wear StudyCOMPLETED

Other records listing Medtronic Minimed, Inc. as applicant

PMA P160017Automated insulin dosing device system, single hormonal control PMA P250012Sensor, Glucose, Invasive, Component of automated insulin delivery system PMA P160007Sensor, glucose, invasive PMA P150001Automated insulin dosing , threshold suspend K261962SmartGuard Technology; Predictive Low Glucose Technology K253743MiniMed Flex pump

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Related Devices (Code: QFG)

K261672twiist Automated Insulin Delivery (AID) SystemDeka Research and Development K253976iLet ACE PumpBeta Bionics, Inc.K253743MiniMed Flex pumpMedtronic Minimed, Inc.K253074Tandem Mobi insulin pump with interoperable technologyTandem Diabetes Care, Inc.K252770iLet ACE PumpBeta Bionics, Inc.K250792t:slim X2 insulin pump with interoperable technologyTandem Diabetes Care, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.