510(k) K130923 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
5F DIGNITY CT TITANIUM PORT
| Applicant | Medical Components, Inc., Harleysville PA, US |
| Decision | Substantially Equivalent, Jul 31, 2013 |
| Received | Apr 3, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130923
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.