K251372
- 510(k) number
- K251372
- Device name
- VersaD Delivery Catheter
- Applicant
- Unity Medical, Inc. MN · US
- Product code
- QJP — Catheter, Percutaneous, Neurovasculature
- Decision date
- 2025-10-24
- Date received
- 2025-05-02
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K251372.pdf
Official FDA record: K251372
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.