K253203
- 510(k) number
- K253203
- Device name
- Retrograde Coronary Sinus Perfusion Cannulae
- Applicant
- Medtronic, Inc. MN · US
- Product code
- DWF — Catheter, Cannula And Tubing, Vascular, Cardiopulmon
- Decision date
- 2026-02-19
- Date received
- 2025-09-26
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 0.3 MB · U.S. public domain
Also available from FDA: K253203.pdf
Official FDA record: K253203
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.