510(k) K973945 ยท DQX Wire, Guide, Catheter
LUGE GUIDE WIRE
| Applicant | Scimed Life Systems, Inc., Maple Grove MN, US |
| Decision | Substantially Equivalent, Jan 12, 1998 |
| Received | Oct 16, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973945
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.