510(k) K913353 ยท DQX Wire, Guide, Catheter
VASCULAR GUIDE WIRE
| Applicant | Advanced Cardiovascular Systems, Inc., Temecula CA, US |
| Decision | Substantially Equivalent, Oct 23, 1991 |
| Received | Jul 26, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913353
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.