510(k) K942103 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
L-CATH CATHETER SYSTEM - PORT L-CATH
| Applicant | Luther Medical Products, Inc., Tustin CA, US |
| Decision | Substantially Equivalent, Jul 26, 1994 |
| Received | May 2, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K942103
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.