510(k) K232737 · LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
PowerPort ClearVUE Slim ECG Enabled Implantable Port; PowerPort ClearVUE isp ECG Enabled Implantable Port; PowerPort isp M.R.I. ECG Enabled Implantable Port; PowerPort Slim ECG Enabled Implantable Port
| Applicant | Bard Peripheral Vascular, Inc., Tempe AZ, US |
| Decision | Substantially Equivalent, Dec 8, 2023 |
| Received | Sep 7, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K232737
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.