K242873
- 510(k) number
- K242873
- Device name
- Ventrax Delivery System
- Applicant
- Merit Medical Systems, Inc. UT · US
- Product code
- DQY — Catheter, Percutaneous
- Decision date
- 2025-01-15
- Date received
- 2024-09-23
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 3.0 MB · U.S. public domain
Also available from FDA: K242873.pdf
Official FDA record: K242873
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.