510(k) K971254 ยท DQX Wire, Guide, Catheter
TRANSEND EX PLATINUM GUIDEWIRE
| Applicant | Boston Scientific Corp, Natick, MA, US |
| Decision | Substantially Equivalent, Jul 1, 1997 |
| Received | Apr 3, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K971254
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.