510(k) K261825 ยท DQY Catheter, Percutaneous
Amplatzer TorqVue LP Delivery System; Amplatzer TorqVue LP Catheter
| Applicant | Abbott, Saint Paul MN, US |
| Decision | Substantially Equivalent, Jul 2, 2026 |
| Received | Jun 2, 2026 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K261825
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.