Ixl Diabetes Management System
FDA 510(k) K031373 · Insulet Corp.
510(k) numberK031373
Submission
- Device name
- Ixl Diabetes Management System
- Applicant
- Insulet Corp.
Beverly, MA, US - Received
- April 30, 2003
- Decision date
- December 19, 2003
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 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
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| 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 |
| K241622 | Extended Reservoir; MiniMed ReservoirLZG · Special | Medtronic Minimed | 07/02/2024SE |
| 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 |
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| K231826 | Omnipod 5 ACE PumpQFG · Traditional | 10/18/2023SE |
| K231824 | SmartBolus CalculatorQRX · Traditional | 10/18/2023SE |
| K223372 | Omnipod GO Insulin Delivery DeviceLZG · Traditional | 04/24/2023SE |
| K222239 | SmartBolus CalculatorQRX · Traditional | 08/19/2022SE |
| K220394 | SmartAdjust(TM) technologyQJI · Traditional | 08/19/2022SE |
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Questions and answers
When was Ixl Diabetes Management System cleared by the FDA?
Ixl Diabetes Management System (K031373) received a 510(k) decision of Substantially Equivalent on December 19, 2003, 233 days after the submission was received.
What is the product code of K031373?
The FDA product code is LZG – Pump, Infusion, Insulin, a Class II (moderate risk) device regulated under 21 CFR 880.5725.