510(k) K232690 · DQY Catheter, Percutaneous
Amulet Steerable Delivery Sheath
| Applicant | ABBOTT MEDICAL, St. Paul MN, US |
| Decision | Substantially Equivalent, Sep 29, 2023 |
| Received | Sep 1, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K232690
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.