510(k) K925979 ยท DQX Wire, Guide, Catheter
DUAL LUMEN L-CATH CATHETER SYSTEM
| Applicant | Luther Medical Products, Inc., Tustin CA, US |
| Decision | Substantially Equivalent, May 27, 1993 |
| Received | Nov 25, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K925979
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.