K241581
- 510(k) number
- K241581
- Device name
- Hemodialysis Catheter
- Applicant
- Haolang Medical USA Corporation WA · US
- Product code
- MSD — Catheter, Hemodialysis, Implanted
- Decision date
- 2025-05-16
- Date received
- 2024-06-03
- Decision
- Unknown
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 0.3 MB · U.S. public domain
Also available from FDA: K241581.pdf
Official FDA record: K241581
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.