510(k) K863178 ยท DQX Wire, Guide, Catheter
UMI STEERABLE TORQUE GUIDE WIRE
| Applicant | Universal Medical Instrument Corp., Ballston Spa NY, US |
| Decision | Substantially Equivalent, Sep 19, 1986 |
| Received | Aug 18, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K863178
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.