K260993
- 510(k) number
- K260993
- Device name
- Amplatzer TorqVue Delivery System
- Applicant
- Abbott MN · US
- Product code
- DQY — Catheter, Percutaneous
- Decision date
- 2026-04-24
- Date received
- 2026-03-26
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K260993.pdf
Official FDA record: K260993
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.