510(k) K260062
- Device
- MODI System
- Applicant
- DreaMed Diabetes, Ltd.
- 510(k) number
- K260062
- Product code
- QRX
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 2026-09-08
- Date received
- 2026-01-08
- Regulation
- 862.1358
- Classification name
- Continuous Glucose Monitor Informed Insulin Dose Calculator
- Medical specialty
- Clinical Chemistry
- Review panel
- Clinical Chemistry
- Device class
- 2
- Clearance type
- Traditional
- Statement or summary
- Summary
- Third party reviewed
- N
Applicant Contact#
- Contact
- Adi Berkovitch
- Address
- 14 Kaplan St. Petah Tikva IL 4920235 4920235
FDA Registration Numbers#
- 3014585508
- 3004753838
Source Documents#
Other 510(k) Records For Product Code QRX#
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K252818 | Dexcom Smart Basal | Dexcom, Inc. | 2025-11-18 |
| K231824 | SmartBolus Calculator | Insulet Corporation | 2023-10-18 |
| K222888 | BlueStar CGM insulin dose calculator | Welldoc, Inc. | 2023-08-11 |
| K222239 | SmartBolus Calculator | Insulet Corporation | 2022-08-19 |
| K203772 | Omnipod 5 SmartBolus Calculator | Insulet Corporation | 2022-01-27 |