510(k) K915723 ยท DQX Wire, Guide, Catheter
.10' HI-TORQUE FLOPPY, INTER. & STAND. GUIDE WIRE
| Applicant | Advanced Cardiovascular Systems, Inc., Santa Clara CA, US |
| Decision | Substantially Equivalent, Jun 9, 1992 |
| Received | Dec 20, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K915723
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.