510(k) K242328 · LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
PowerPort ClearVUE Slim Implantable Ports and PowerPort ClearVUE Slim Implantable Ports
| Applicant | Bard Access Systems, Inc., Salt Lake Ciy, UT, US |
| Decision | Substantially Equivalent, Oct 31, 2024 |
| Received | Aug 6, 2024 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K242328
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.