510(k) K880571 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
CATH-TECH PORT IMPLANTABLE VASCULAR ACCESS SYSTEM
| Applicant | Catheter Technology Corp., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Mar 4, 1988 |
| Received | Feb 10, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880571
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.