510(k) K970494 · DQX Wire, Guide, Catheter
HANNIBAL GUIDEWIRE
| Applicant | Schneider (Europe) GmbH, Bülach, CH |
| Decision | Substantially Equivalent, May 9, 1997 |
| Received | Feb 10, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970494
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.