510(k) K951109 ยท DQX Wire, Guide, Catheter
C-THRU CORONARY GUIDE WIRE
| Applicant | Schneider (Europe) GmbH, Bulach, SE |
| Decision | Substantially Equivalent, Jun 8, 1995 |
| Received | Mar 10, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K951109
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.