510(k) K922410 ยท DQX Wire, Guide, Catheter
SCIMED AVENUE CORONARY GUIDEWIRE INSERTION TOOL
| Applicant | Scimed Life Systems, Inc., Maple Grove MN, US |
| Decision | Substantially Equivalent, Jul 23, 1992 |
| Received | May 21, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K922410
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.