K253741
- 510(k) number
- K253741
- Device name
- VStick Vascular Access Set
- Applicant
- Argon Medical Devices, Inc. TX · US
- Product code
- DYB — Introducer, Catheter
- Decision date
- 2025-12-15
- Date received
- 2025-11-24
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 3.1 MB · U.S. public domain
Also available from FDA: K253741.pdf
Official FDA record: K253741
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.