510(k) K930473 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
ONECATH L-CATH CATHETER SYSTEM
| Applicant | Luther Medical Products, Inc., Tustin CA, US |
| Decision | Unknown, Apr 7, 1994 |
| Received | Jan 28, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K930473
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.