510(k) K950352 ยท DQX Wire, Guide, Catheter
PRECEDER GUIDEWIRE
| Applicant | Boston Scientific Corp, Watertown MA, US |
| Decision | Substantially Equivalent, Apr 28, 1995 |
| Received | Jan 30, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K950352
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.