510(k) K030636 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
C-PORT
| Applicant | Clinisurg Vascular Products, LLC, Dallas TX, US |
| Decision | Substantially Equivalent, Jun 5, 2003 |
| Received | Feb 28, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K030636
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.