510(k) K241538 ยท DQY Catheter, Percutaneous
TriClip Steerable Guide Catheter
| Applicant | ABBOTT MEDICAL, St. Paul MN, US |
| Decision | Substantially Equivalent, Aug 26, 2024 |
| Received | May 30, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241538
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.