510(k) K200721 ยท DQY Catheter, Percutaneous
Agilis HisPro Steerable Catheter With Electrodes
| Applicant | Abbott (St. Jude Medical), Sylmar CA, US |
| Decision | Substantially Equivalent, Jun 3, 2020 |
| Received | Mar 19, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K200721
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.