510(k) K960350 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
THERAPORT VASCULAR ACCESS SYSTEM; MODEL 1001, 1002, 1601, 1602
| Applicant | Biocontrol Technology, Inc., Indiana PA, US |
| Decision | Substantially Equivalent, Apr 15, 1996 |
| Received | Jan 25, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960350
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.