K241622
- 510(k) number
- K241622
- Device name
- Extended Reservoir; MiniMed Reservoir
- Applicant
- Medtronic Minimed CA · US
- Product code
- LZG — Pump, Infusion, Insulin
- Decision date
- 2024-07-02
- Date received
- 2024-06-05
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 1.1 MB · U.S. public domain
Also available from FDA: K241622.pdf
Official FDA record: K241622
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.