510(k) K260993 ยท DQY Catheter, Percutaneous
Amplatzer TorqVue Delivery System
| Applicant | Abbott, Saint Paul MN, US |
| Decision | Substantially Equivalent, Apr 24, 2026 |
| Received | Mar 26, 2026 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K260993
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.