K240748
- 510(k) number
- K240748
- Device name
- nextaro® v, 20/20
- Applicant
- Sfm Medical Devices GmbH DE
- Product code
- LHI — Set, I.V. Fluid Transfer
- Decision date
- 2024-04-16
- Date received
- 2024-03-19
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 0.3 MB · U.S. public domain
Also available from FDA: K240748.pdf
Official FDA record: K240748
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.