510(k) K875213 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
SURECATH - ITP II PERCUTANEOUS PORT ACCESS DEVICE
| Applicant | Titan Medical, Inc., Arden Hills MN, US |
| Decision | Substantially Equivalent, Mar 3, 1988 |
| Received | Dec 18, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K875213
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.