K242390
- 510(k) number
- K242390
- Device name
- Novum IQ Syringe Pump (40800BAXUS)
- Applicant
- Baxter Healthcare Corporation IL · US
- Product code
- FRN — Pump, Infusion
- Decision date
- 2024-09-05
- Date received
- 2024-08-12
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K242390.pdf
Official FDA record: K242390
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.