510(k) K251253 · LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
PowerPort isp Implantable Port; PowerPort Slim Implantable Port; PowerPort M.R.I. Implantable Port; PowerPort M.R.I. isp Implantable Port
| Applicant | Bard Access Systems, Inc., Salt Lake Ciy, UT, US |
| Decision | Substantially Equivalent, Jun 18, 2025 |
| Received | Apr 23, 2025 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K251253
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.