510(k) K925381 ยท DQX Wire, Guide, Catheter
ACS HI-TORQUE BALANCE(TM) GUIDE WIRE
| Applicant | Advanced Cardiovascular Systems, Inc., Santa Clara CA, US |
| Decision | Substantially Equivalent, Feb 12, 1993 |
| Received | Oct 23, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K925381
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.