K232722
- 510(k) number
- K232722
- Device name
- endo.digital Platform
- Applicant
- DreaMed Diabetes, Ltd. IL
- Product code
- QCC — Insulin Pump Therapy Adjustment Calculator For Healt
- Decision date
- 2023-10-03
- Date received
- 2023-09-05
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Clinical Chemistry
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K232722.pdf
Official FDA record: K232722
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.