510(k) K934122 ยท DQX Wire, Guide, Catheter
SCIMED TRANSEND EX STEERABLE GUIDE WIRE AND ACCESSORIES
| Applicant | Scimed Peripheral Interventions, Plymouth MN, US |
| Decision | Substantially Equivalent, Oct 7, 1993 |
| Received | Aug 25, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K934122
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.