510(k) K934167 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
IPI DUAL LUMEN PORT
| Applicant | Pudenz-Schulte Medical Research Corp., Goleta CA, US |
| Decision | Substantially Equivalent, Jul 14, 1994 |
| Received | Aug 27, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K934167
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.