510(k) K950315 ยท LKG Port & Catheter, Implanted, Subcutaneous, Intraventricular
CORDIS CSF RESERVOIR
| Applicant | Cordis Corp., Miami FL, US |
| Decision | Unknown, May 9, 1995 |
| Received | Jan 26, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K950315
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.