K252390
- 510(k) number
- K252390
- Device name
- Telescope Guide Extension Catheter
- Applicant
- Medtronic, Ireland IE
- Product code
- DQY — Catheter, Percutaneous
- Decision date
- 2025-10-29
- Date received
- 2025-07-31
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 0.0 MB · U.S. public domain
Also available from FDA: K252390.pdf
Official FDA record: K252390
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.