K240650
- 510(k) number
- K240650
- Device name
- LungProtect
- Applicant
- Traferox Technologies, Inc. CA
- Product code
- KDN — System, Perfusion, Kidney
- Decision date
- 2024-11-26
- Date received
- 2024-03-07
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K240650.pdf
Official FDA record: K240650
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.