510(k) K902153 ยท DQX Wire, Guide, Catheter
TEFLON COATED GUIDEWIRE
| Applicant | Guidewire Technologies, Inc., Salem NH, US |
| Decision | Substantially Equivalent, Jul 31, 1990 |
| Received | May 16, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902153
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.