K243852
- 510(k) number
- K243852
- Device name
- Elfor-L
- Applicant
- Elfi-Tech , Ltd. IL
- Product code
- DPW — Flowmeter, Blood, Cardiovascular
- Decision date
- 2025-04-14
- Date received
- 2024-12-16
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K243852.pdf
Official FDA record: K243852
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.