510(k) K860430 ยท DQX Wire, Guide, Catheter
THE NAVIGATOR STEERABLE GUIDE WIRE
| Applicant | Meadox Surgimed, Inc., Oakland NJ, US |
| Decision | Substantially Equivalent, Jul 18, 1986 |
| Received | Feb 4, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860430
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.