K241976
- 510(k) number
- K241976
- Device name
- nextaro® va, 15mm, 5µm
- Applicant
- Sfm Medical Devices GmbH DE
- Product code
- LHI — Set, I.V. Fluid Transfer
- Decision date
- 2024-09-06
- Date received
- 2024-07-05
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K241976.pdf
Official FDA record: K241976
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.