510(k) K980090 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
ONECATH, L-CATH CATHETER SYSTEM, MODEL OC-(16-22 GA., 5CM-60CM)
| Applicant | Luther Medical Products, Inc., Newport Beach CA, US |
| Decision | Substantially Equivalent, Mar 24, 1998 |
| Received | Jan 9, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980090
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.