510(k) K910969 ยท DQX Wire, Guide, Catheter
TORQUE DEVICE FOR A GUIDE WIRE
| Applicant | Terumo Corp., Somerset NJ, US |
| Decision | Substantially Equivalent, May 16, 1991 |
| Received | Mar 6, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910969
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.