K244059
- 510(k) number
- K244059
- Device name
- HydroMID 5F Dual Lumen Midline Catheter - Basic Kit (70006102); HydroMID 5F Dual Lumen Midline Catheter - Max Barrier Kit (70006104); HydroMID 5F Dual Lumen Midline Catheter - Mobile Max Barrier Kit (90006104)
- Applicant
- Access Vascular, Inc. MD · US
- Product code
- FOZ — Catheter, Intravascular, Therapeutic, Short-Term Les
- Decision date
- 2025-03-27
- Date received
- 2024-12-31
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K244059.pdf
Official FDA record: K244059
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.