510(k) K013092 ยท DQX Wire, Guide, Catheter
HI-TOQUE WHISPER LS AND MS GUIDE WIRE WITH HYDROCOAT HYDROPHILIC COATING
| Applicant | Guidant Corp., Temecula CA, US |
| Decision | Substantially Equivalent, Dec 13, 2001 |
| Received | Sep 17, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013092
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.