510(k) K980119 ยท DQX Wire, Guide, Catheter
ACS HI-TORQUE WHOLEY SUPRA CORE GUIDE WIRE
| Applicant | Guidant Corp., Santa Clara CA, US |
| Decision | Substantially Equivalent, Mar 20, 1998 |
| Received | Jan 13, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980119
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.