510(k) K890959 ยท DQX Wire, Guide, Catheter
GUIDEWIRE
| Applicant | Guidewire Technologies, Inc., Salem NH, US |
| Decision | Substantially Equivalent, Sep 12, 1989 |
| Received | Feb 27, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890959
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.