510(k) K941710 ยท DQX Wire, Guide, Catheter
SCIMED TRANSEND STEERABLE GUIDE WIRE AND ACCESSORIES
| Applicant | Scimed Peripheral Interventions, Plymouth MN, US |
| Decision | Substantially Equivalent, Sep 1, 1994 |
| Received | Apr 6, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K941710
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.