K242115
- 510(k) number
- K242115
- Device name
- Plum Duo Precision IV Pump
- Applicant
- Icu Medical, Inc. IL · US
- Product code
- FRN — Pump, Infusion
- Decision date
- 2025-04-02
- Date received
- 2024-07-19
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 1.1 MB · U.S. public domain
Also available from FDA: K242115.pdf
Official FDA record: K242115
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.