510(k) K022357 ยท DQX Wire, Guide, Catheter
TRANSEND 300 ES GUIDEWIRE, MODEL 46-814 & TRANSEND 300 FLOPPY GUIDEWIRE, MODEL 46-815
| Applicant | Boston Scientific, Target, Fremont CA, US |
| Decision | Substantially Equivalent, Oct 16, 2002 |
| Received | Jul 19, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K022357
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.