510(k) K935232 ยท DQX Wire, Guide, Catheter
HYDROTORQUE GUIDE WIRE
| Applicant | Kingston Technologies, Inc., Dayton NJ, US |
| Decision | Substantially Equivalent, Jul 20, 1994 |
| Received | Nov 1, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K935232
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.