510(k) K984394 ยท DQX Wire, Guide, Catheter
ACS HI-TORQUE WIGGLE GUIDE WIRE WITH MICROGLIDE COATING
| Applicant | Guidant Corp., Santa Clara CA, US |
| Decision | Substantially Equivalent, Mar 8, 1999 |
| Received | Dec 8, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K984394
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.