Extended Reservoir; MiniMed Reservoir
FDA 510(k) K241622 · Medtronic Minimed
510(k) numberK241622
Submission
- Device name
- Extended Reservoir; MiniMed Reservoir
- Applicant
- Medtronic Minimed
Northridge, CA, US - Received
- June 5, 2024
- Decision date
- July 2, 2024
- Decision
- Substantially Equivalent (SESE)
- Type
- Special 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- LZG – Pump, Infusion, Insulin
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 880.5725
- Specialty
- General Hospital
Other 510(k)s with product code LZG
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K262153 | Pivot Insulin Delivery SystemLZG · Traditional | Modular Medical, Inc. | 09/02/2026SE |
| K253534 | Pivot Insulin Delivery SystemLZG · Traditional | Modular Medical | 04/08/2026SE |
| K240158 | Modular Medical MODD1 Insulin Delivery SystemLZG · Traditional | Modular Medical, Inc. | 09/04/2024SE |
| K223372 | Omnipod GO Insulin Delivery DeviceLZG · Traditional | Insulet Corporation | 04/24/2023SE |
| K210714 | Extended ReservoirLZG · Traditional | Medtronic Minimed, Inc. | 04/06/2022SE |
| K211575 | Omnipod® Insulin Management System, Omnipod DASH® Insulin Management SystemLZG · Traditional | Insulet Corporation | 08/13/2021SE |
| K192659 | Omnipod Insulin Management System, Omnipod DASH Insulin Management SystemLZG · Traditional | Insulet Corporation | 10/21/2019SE |
| K182630 | Omnipod Insulin Management System, Omnipod DASH Insulin Management SystemLZG · Traditional | Insulet Corporation | 01/08/2019SE |
| K180045 | Omnipod DASH Insulin Management SystemLZG · Traditional | Insulet Corporation | 06/01/2018SE |
| K162296 | OmniPod Insulin Management SystemLZG · Traditional | Insulet Corporation | 04/18/2017SE |
More from Insulet Corporation
| 510(k) | Device | Decision |
|---|---|---|
| K261962 | SmartGuard Technology; Predictive Low Glucose TechnologyQJI · Special | 07/09/2026SE |
| K253743 | MiniMed Flex pumpQFG · Traditional | 03/12/2026SE |
| K253701 | SmartGuard Technology; Predictive Low Glucose TechnologyQJI · Traditional | 02/03/2026SE |
| K253470 | MiniMed 780G Insulin Pump (MMT-1884); MiniMed 780G Insulin Pump Kit (MMT-1894)QFG · Traditional | 01/15/2026SE |
| K253585 | SmartGuard technology; Predictive Low Glucose technologyQJI · Traditional | 01/14/2026SE |
| K253512 | MiniMed Go AppNDC · Traditional | 01/08/2026SE |
| K251217 | SmartGuard technology; Predictive Low Glucose technologyQJI · Traditional | 08/29/2025SE |
| K251032 | MiniMed 780G insulin pumpQFG · Traditional | 07/01/2025SE |
| K242775 | InPen System App (MMT-8060 (iOS), MMT-8061 (Android))NDC · Traditional | 11/12/2024SE |
| K210714 | Extended ReservoirLZG · Traditional | 04/06/2022SE |
Questions and answers
When was Extended Reservoir; MiniMed Reservoir cleared by the FDA?
Extended Reservoir; MiniMed Reservoir (K241622) received a 510(k) decision of Substantially Equivalent on July 2, 2024, 27 days after the submission was received.
What is the product code of K241622?
The FDA product code is LZG – Pump, Infusion, Insulin, a Class II (moderate risk) device regulated under 21 CFR 880.5725.