Class Class II
MiniMed 780G insulin pump (K251032)
Description
MiniMed 780G insulin pump by Medtronic Minimed, Inc., an FDA 510(k) cleared clinical chemistry device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK251032
Clearance Date2025-07-01
Clearance TypeTraditional
Product CodeQFG
Regulation Number880.5730
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K251032
A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. MiniMed 780G insulin pump (K251032) cites 2 predicate devices and is itself cited by 1 later device.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K242775 | InPen System App (MMT-8060 (iOS), MMT-8061 (Android)) | Medtronic Minimed | 2024 |
| K232380 | t:slim X2 Insulin Pump with Interoperable Technology | Tandem Diabetes Care, Inc. | 2023 |
Later devices that cite this one as their predicate
| K number | Device | Applicant | Year |
|---|---|---|---|
| K253743 | MiniMed Flex pump | Medtronic Minimed, Inc. | 2026 |
Trace the full predicate network for K251032
A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.