510(k) K902152 ยท DQX Wire, Guide, Catheter
MOVABLE CORE GUIDEWIRE
| Applicant | Guidewire Technologies, Inc., Salem NH, US |
| Decision | Substantially Equivalent, Jul 31, 1990 |
| Received | May 15, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902152
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.