K252402
- 510(k) number
- K252402
- Device name
- Midline Catheter
- Applicant
- Terumo Medical Products (Hangzhou) Co., Ltd. CN
- Product code
- PND — Midline Catheter
- Decision date
- 2025-12-18
- Date received
- 2025-07-31
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K252402.pdf
Official FDA record: K252402
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.