K242328
- 510(k) number
- K242328
- Device name
- PowerPort ClearVUE Slim Implantable Ports and PowerPort ClearVUE Slim Implantable Ports
- Applicant
- Bard Access Systems, Inc. UT · US
- Product code
- LJT — Port & Catheter, Implanted, Subcutaneous, Intravascu
- Decision date
- 2024-10-31
- Date received
- 2024-08-06
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K242328.pdf
Official FDA record: K242328
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.